ADIPOQ - adiponectin, C1Q and collagen domain containing Gene

Also Known as ACDC; ADPN; APM1; APM-1; GBP28; ACRP30; ADIPQTL1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 9370

About ADIPOQ

Cytogenetic location: 3q27.3 Genomic coordinates (GRCh38): 3:186,842,710-186,858,463 (from NCBI)

This gene has 2 transcripts (splice variants), 166 orthologues, 23 paralogues and is associated with 1 phenotype. Restricted expression toward fat (RPKM 648.8).

Summary

This gene is expressed in adipose tissue exclusively. It encodes a protein with similarity to collagens X and VIII and complement factor C1q. The encoded protein circulates in the plasma and is involved with metabolic and hormonal processes. Mutations in this gene are associated with Adiponectin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Apr 2010]

ADIPOQ Products (4)

mRNA Protein Name
NM_001177800.2 NP_001171271.1 adiponectin precursor
NM_004797.4 NP_004788.1 adiponectin precursor
NM_001177800.2 NP_001171271.1 adiponectin precursor
NM_004797.4 NP_004788.1 adiponectin precursor
Molecular Function GO Annotation Evidence References Source
enables hormone activity IDA
IDA: Inferred from direct assay
11222466 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
12070119 GOA
enables protein homodimerization activity IPI
IPI: Inferred from physical interaction
12021245 GOA
enables sialic acid binding IDA
IDA: Inferred from direct assay
19855092 GOA
Biological Process GO Annotation Evidence References Source
involved in low-density lipoprotein particle clearance IDA
IDA: Inferred from direct assay
11222466 GOA
involved in negative regulation of DNA biosynthetic process IDA
IDA: Inferred from direct assay
12070119 GOA
involved in negative regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
18431508 GOA
involved in negative regulation of ERK1 and ERK2 cascade IDA
IDA: Inferred from direct assay
12070119 GOA
involved in negative regulation of blood pressure IDA
IDA: Inferred from direct assay
17327472 GOA
involved in negative regulation of canonical NF-kappaB signal transduction IDA
IDA: Inferred from direct assay
10982546 GOA
involved in negative regulation of fat cell differentiation IDA
IDA: Inferred from direct assay
12021245 GOA
involved in negative regulation of granulocyte differentiation IDA
IDA: Inferred from direct assay
10961870 GOA
involved in negative regulation of heterotypic cell-cell adhesion IDA
IDA: Inferred from direct assay
10604883 GOA
involved in negative regulation of intracellular protein transport IDA
IDA: Inferred from direct assay
18431508 GOA
acts upstream of negative regulation of low-density lipoprotein receptor activity IDA
IDA: Inferred from direct assay
11222466 GOA
involved in negative regulation of macrophage derived foam cell differentiation IDA
IDA: Inferred from direct assay
11222466 GOA
involved in negative regulation of macrophage differentiation IDA
IDA: Inferred from direct assay
10961870 GOA
involved in negative regulation of phagocytosis IDA
IDA: Inferred from direct assay
10961870 GOA
involved in negative regulation of platelet-derived growth factor receptor signaling pathway IDA
IDA: Inferred from direct assay
12070119 GOA
involved in negative regulation of protein autophosphorylation IDA
IDA: Inferred from direct assay
12070119 GOA
involved in negative regulation of receptor binding IDA
IDA: Inferred from direct assay
12070119 GOA
involved in negative regulation of synaptic transmission IDA
IDA: Inferred from direct assay
17327472 GOA
involved in negative regulation of tumor necrosis factor production IDA
IDA: Inferred from direct assay
10961870 GOA
involved in negative regulation of tumor necrosis factor-mediated signaling pathway IDA
IDA: Inferred from direct assay
10604883 GOA
involved in negative regulation of vascular associated smooth muscle cell migration IDA
IDA: Inferred from direct assay
12070119 GOA
involved in negative regulation of vascular associated smooth muscle cell proliferation IDA
IDA: Inferred from direct assay
12070119 GOA
involved in positive regulation of cAMP-dependent protein kinase activity IDA
IDA: Inferred from direct assay
18431508 GOA
involved in positive regulation of cAMP/PKA signal transduction IDA
IDA: Inferred from direct assay
10982546 GOA
involved in positive regulation of cholesterol efflux IDA
IDA: Inferred from direct assay
18703020 GOA
involved in positive regulation of interleukin-8 production IDA
IDA: Inferred from direct assay
19524870 GOA
involved in positive regulation of lipid transporter activity IDA
IDA: Inferred from direct assay
18703020 GOA
involved in positive regulation of monocyte chemotactic protein-1 production IDA
IDA: Inferred from direct assay
19524870 GOA
involved in positive regulation of myeloid cell apoptotic process IDA
IDA: Inferred from direct assay
10961870 GOA
involved in positive regulation of protein phosphorylation IDA
IDA: Inferred from direct assay
18431508 GOA
involved in positive regulation of renal albumin absorption IDA
IDA: Inferred from direct assay
18431508 GOA
involved in protein localization to plasma membrane IDA
IDA: Inferred from direct assay
18431508 GOA
involved in regulation of glucose metabolic process IDA
IDA: Inferred from direct assay
17327472 GOA
involved in response to tumor necrosis factor IDA
IDA: Inferred from direct assay
10604883 GOA
Cellular Component GO Annotation Evidence References Source
located in cell surface IDA
IDA: Inferred from direct assay
10982546 GOA
located in extracellular space IDA
IDA: Inferred from direct assay
10403784 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ADIPOQ Protein Structure

Collagen

Collagen: pfam01391 (50 - 105)

C1Q

C1Q: smart00110 (105 - 241)

  • 0
  • 100
  • 200
  • 244 a.a.
Protein Preferred Names Protein Names

adiponectin

  • 30 kDa adipocyte complement-related protein

ADIPOQ Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ADIPOQ Q15848 HSD17B11 Homo sapiens Q8NBQ5 32296183
Intra
ADIPOQ Q15848 HSD17B11 Homo sapiens Q8NBQ5 32296183
Intra
ADIPOQ Q15848 HSD17B11 Homo sapiens Q8NBQ5 32296183
Intra
ADIPOQ Q15848 SYAP1 Homo sapiens Q96A49 32296183
Intra
ADIPOQ Q15848 SYAP1 Homo sapiens Q96A49 32296183
Intra
ADIPOQ Q15848 SYAP1 Homo sapiens Q96A49 32296183
Intra
ADIPOQ Q15848 NEMP1 Homo sapiens O14524-2 32296183
Intra
ADIPOQ Q15848 NEMP1 Homo sapiens O14524-2 32296183
Intra
ADIPOQ Q15848 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
ADIPOQ Q15848 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
ADIPOQ Q15848 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
ADIPOQ Q15848 TMEM35A Homo sapiens Q53FP2 32296183
Intra
ADIPOQ Q15848 TMEM35A Homo sapiens Q53FP2 32296183
Intra
ADIPOQ Q15848 TMEM35A Homo sapiens Q53FP2 32296183
Intra
ADIPOQ Q15848 TMEM179B Homo sapiens Q7Z7N9 32296183
Intra
ADIPOQ Q15848 TMEM179B Homo sapiens Q7Z7N9 32296183
Intra
ADIPOQ Q15848 TMEM179B Homo sapiens Q7Z7N9 32296183
Intra
ADIPOQ Q15848 CLEC2D Homo sapiens Q9UHP7-3 32296183
Intra
ADIPOQ Q15848 CLEC2D Homo sapiens Q9UHP7-3 32296183
Intra
ADIPOQ Q15848 CLEC2D Homo sapiens Q9UHP7-3 32296183
Intra
ADIPOQ Q15848 MFF Homo sapiens Q9GZY8-5 32296183
Intra
ADIPOQ Q15848 MFF Homo sapiens Q9GZY8-5 32296183
Intra
ADIPOQ Q15848 MFF Homo sapiens Q9GZY8-5 32296183
Intra
ADIPOQ Q15848 SLC22A23 Homo sapiens A1A5C7-2 32296183
Intra
ADIPOQ Q15848 SLC22A23 Homo sapiens A1A5C7-2 32296183
Intra
ADIPOQ Q15848 SYNE4 Homo sapiens Q8N205-2 32296183
Intra
ADIPOQ Q15848 SYNE4 Homo sapiens Q8N205-2 25910212
Intra
ADIPOQ Q15848 SYNE4 Homo sapiens Q8N205-2 32296183
Intra
ADIPOQ Q15848 SYNE4 Homo sapiens Q8N205-2 25910212
Intra
ADIPOQ Q15848 SYNE4 Homo sapiens Q8N205-2 25910212
Intra
ADIPOQ Q15848 SYNE4 Homo sapiens Q8N205-2 32296183
Intra
ADIPOQ Q15848 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
ADIPOQ Q15848 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
ADIPOQ Q15848 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
ADIPOQ Q15848 TMPRSS2 Homo sapiens O15393-2 32296183
Intra
ADIPOQ Q15848 TMPRSS2 Homo sapiens O15393-2 32296183
Intra
ADIPOQ Q15848 MS4A3 Homo sapiens Q96HJ5 32296183
Intra
ADIPOQ Q15848 MS4A3 Homo sapiens Q96HJ5 32296183
Intra
ADIPOQ Q15848 MS4A3 Homo sapiens Q96HJ5 32296183
Intra
ADIPOQ Q15848 ASGR2 Homo sapiens P07307-3 32296183
Intra
ADIPOQ Q15848 ASGR2 Homo sapiens P07307-3 32296183
Intra
ADIPOQ Q15848 CD200R1 Homo sapiens Q8TD46-4 32296183
Intra
ADIPOQ Q15848 CD200R1 Homo sapiens Q8TD46-4 32296183
Intra
ADIPOQ Q15848 CD200R1 Homo sapiens Q8TD46-4 32296183
Intra
ADIPOQ Q15848 PROKR2 Homo sapiens Q8NFJ6 32296183
Intra
ADIPOQ Q15848 PROKR2 Homo sapiens Q8NFJ6 32296183
Intra
ADIPOQ Q15848 PROKR2 Homo sapiens Q8NFJ6 32296183
Intra
ADIPOQ Q15848 AQP6 Homo sapiens Q13520 32296183
Intra
ADIPOQ Q15848 AQP6 Homo sapiens Q13520 32296183
Intra
ADIPOQ Q15848 GPR152 Homo sapiens Q8TDT2 32296183
Intra
ADIPOQ Q15848 GPR152 Homo sapiens Q8TDT2 32296183
Intra
ADIPOQ Q15848 GPR152 Homo sapiens Q8TDT2 32296183
Intra
ADIPOQ Q15848 SLC35E3 Homo sapiens Q7Z769 32296183
Intra
ADIPOQ Q15848 SLC35E3 Homo sapiens Q7Z769 32296183
Intra
ADIPOQ Q15848 SLC35E3 Homo sapiens Q7Z769 32296183
Intra
ADIPOQ Q15848 SCN3B Homo sapiens Q9NY72 32296183
Intra
ADIPOQ Q15848 SCN3B Homo sapiens Q9NY72 32296183
Intra
ADIPOQ Q15848 SCN3B Homo sapiens Q9NY72 32296183
Intra
ADIPOQ Q15848 MUC1 Homo sapiens P15941-11 32296183
Intra
ADIPOQ Q15848 MUC1 Homo sapiens P15941-11 32296183
Intra
ADIPOQ Q15848 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
ADIPOQ Q15848 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
ADIPOQ Q15848 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
ADIPOQ Q15848 CAMLG Homo sapiens P49069 32296183
Intra
ADIPOQ Q15848 CAMLG Homo sapiens P49069 32296183
Intra
ADIPOQ Q15848 SIGLEC12 Homo sapiens Q96PQ1 32296183
Intra
ADIPOQ Q15848 SIGLEC12 Homo sapiens Q96PQ1 32296183
Intra
ADIPOQ Q15848 SIGLEC12 Homo sapiens Q96PQ1 32296183
Intra
ADIPOQ Q15848 TRIM35 Homo sapiens Q9UPQ4-2 32296183
Intra
ADIPOQ Q15848 TRIM35 Homo sapiens Q9UPQ4-2 32296183
Intra
ADIPOQ Q15848 TRIM35 Homo sapiens Q9UPQ4-2 32296183
Intra
ADIPOQ Q15848 BTNL9 Homo sapiens Q6UXG8-3 32296183
Intra
ADIPOQ Q15848 BTNL9 Homo sapiens Q6UXG8-3 32296183
Intra
ADIPOQ Q15848 BTNL9 Homo sapiens Q6UXG8-3 32296183
Intra
ADIPOQ Q15848 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
ADIPOQ Q15848 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
ADIPOQ Q15848 CPLX4 Homo sapiens Q7Z7G2 32296183
Intra
ADIPOQ Q15848 GPR42 Homo sapiens O15529 32296183
Intra
ADIPOQ Q15848 GPR42 Homo sapiens O15529 32296183
Intra
ADIPOQ Q15848 FAM209A Homo sapiens Q5JX71 32296183
Intra
ADIPOQ Q15848 FAM209A Homo sapiens Q5JX71 32296183
Intra
ADIPOQ Q15848 FAM209A Homo sapiens Q5JX71 32296183
Intra
ADIPOQ Q15848 CLDN9 Homo sapiens O95484 32296183
Intra
ADIPOQ Q15848 CLDN9 Homo sapiens O95484 32296183
Intra
ADIPOQ Q15848 AMIGO1 Homo sapiens Q86WK6 32296183
Intra
ADIPOQ Q15848 AMIGO1 Homo sapiens Q86WK6 32296183
Intra
ADIPOQ Q15848 AMIGO1 Homo sapiens Q86WK6 32296183
Intra
ADIPOQ Q15848 CYBC1 Homo sapiens Q9BQA9 32296183
Intra
ADIPOQ Q15848 CYBC1 Homo sapiens Q9BQA9 32296183
Intra
ADIPOQ Q15848 CYBC1 Homo sapiens Q9BQA9 32296183
Intra
ADIPOQ Q15848 CNR2 Homo sapiens P34972 32296183
Intra
ADIPOQ Q15848 CNR2 Homo sapiens P34972 32296183
Intra
ADIPOQ Q15848 MFSD6 Homo sapiens Q6ZSS7 32296183
Intra
ADIPOQ Q15848 MFSD6 Homo sapiens Q6ZSS7 32296183
Intra
ADIPOQ Q15848 MFSD6 Homo sapiens Q6ZSS7 32296183
Intra
ADIPOQ Q15848 FCGR1A Homo sapiens P12314 32296183
Intra
ADIPOQ Q15848 FCGR1A Homo sapiens P12314 32296183
Intra
ADIPOQ Q15848 CLEC10A Homo sapiens Q8IUN9 32296183
Intra
ADIPOQ Q15848 CLEC10A Homo sapiens Q8IUN9 32296183
Intra
ADIPOQ Q15848 CLEC10A Homo sapiens Q8IUN9 32296183
Intra
ADIPOQ Q15848 SGTA Homo sapiens O43765 25910212
Intra
ADIPOQ Q15848 SGTA Homo sapiens O43765 32296183
Intra
ADIPOQ Q15848 SGTA Homo sapiens O43765 25910212
Intra
ADIPOQ Q15848 SGTA Homo sapiens O43765 25910212
Intra
ADIPOQ Q15848 SGTA Homo sapiens O43765 32296183
Intra
ADIPOQ Q15848 FASN Homo sapiens P49327 32296183
Intra
ADIPOQ Q15848 FASN Homo sapiens P49327 32296183
Intra
ADIPOQ Q15848 MFSD14B Homo sapiens Q5SR56 32296183
Intra
ADIPOQ Q15848 MFSD14B Homo sapiens Q5SR56 32296183
Intra
ADIPOQ Q15848 MFSD14B Homo sapiens Q5SR56 32296183
Intra
ADIPOQ Q15848 IFNGR2 Homo sapiens P38484 32296183
Intra
ADIPOQ Q15848 FKBP7 Homo sapiens Q9Y680 32296183
Intra
ADIPOQ Q15848 FKBP7 Homo sapiens Q9Y680 32296183
Intra
ADIPOQ Q15848 FKBP7 Homo sapiens Q9Y680 32296183
Intra
ADIPOQ Q15848 PVR Homo sapiens P15151 32296183
Intra
ADIPOQ Q15848 PVR Homo sapiens P15151 32296183
Intra
ADIPOQ Q15848 KCNK5 Homo sapiens O95279 32296183
Intra
ADIPOQ Q15848 KCNK5 Homo sapiens O95279 32296183
Intra
ADIPOQ Q15848 TNFSF14 Homo sapiens O43557 32296183
Intra
ADIPOQ Q15848 TNFSF14 Homo sapiens O43557 32296183
Intra
ADIPOQ Q15848 MRM1 Homo sapiens Q6IN84 32296183
Intra
ADIPOQ Q15848 MRM1 Homo sapiens Q6IN84 32296183
Intra
ADIPOQ Q15848 MRM1 Homo sapiens Q6IN84 32296183
Intra
ADIPOQ Q15848 PEX12 Homo sapiens O00623 32296183
Intra
ADIPOQ Q15848 PEX12 Homo sapiens O00623 32296183
Intra
ADIPOQ Q15848 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
ADIPOQ Q15848 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
ADIPOQ Q15848 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
ADIPOQ Q15848 BIK Homo sapiens Q13323 32296183
Intra
ADIPOQ Q15848 BIK Homo sapiens Q13323 32296183
Intra
ADIPOQ Q15848 COQ9 Homo sapiens O75208 32296183
Intra
ADIPOQ Q15848 COQ9 Homo sapiens O75208 32296183
Intra
ADIPOQ Q15848 SGTB Homo sapiens Q96EQ0 32296183
Intra
ADIPOQ Q15848 SGTB Homo sapiens Q96EQ0 32296183
Intra
ADIPOQ Q15848 SGTB Homo sapiens Q96EQ0 32296183
Intra
ADIPOQ Q15848 KEL Homo sapiens P23276 32296183
Intra
ADIPOQ Q15848 KEL Homo sapiens P23276 32296183
Intra
ADIPOQ Q15848 BCL2L13 Homo sapiens Q9BXK5 32296183
Intra
ADIPOQ Q15848 BCL2L13 Homo sapiens Q9BXK5 32296183
Intra
ADIPOQ Q15848 BCL2L13 Homo sapiens Q9BXK5 32296183
Intra
ADIPOQ Q15848 KASH5 Homo sapiens Q8N6L0 25910212
Intra
ADIPOQ Q15848 KASH5 Homo sapiens Q8N6L0 25910212
Intra
ADIPOQ Q15848 KASH5 Homo sapiens Q8N6L0 25910212
Intra
ADIPOQ Q15848 CD79A Homo sapiens P11912 32296183
Intra
ADIPOQ Q15848 CD79A Homo sapiens P11912 32296183
Intra
ADIPOQ Q15848 BSND Homo sapiens Q8WZ55 32296183
Intra
ADIPOQ Q15848 BSND Homo sapiens Q8WZ55 32296183
Intra
ADIPOQ Q15848 BSND Homo sapiens Q8WZ55 32296183
Intra
ADIPOQ Q15848 BNIP3L Homo sapiens O60238 25910212
Intra
ADIPOQ Q15848 BNIP3L Homo sapiens O60238 25910212
Intra
ADIPOQ Q15848 BNIP3L Homo sapiens O60238 25910212
Intra
ADIPOQ Q15848 ERP29 Homo sapiens P30040 32296183
Intra
ADIPOQ Q15848 ERP29 Homo sapiens P30040 32296183
Intra
ADIPOQ Q15848 CCDC107 Homo sapiens Q8WV48 32296183
Intra
ADIPOQ Q15848 CCDC107 Homo sapiens Q8WV48 32296183
Intra
ADIPOQ Q15848 CCDC107 Homo sapiens Q8WV48 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant ADIPOQ Proteins

Cat. No. Product Name Accession Purity
HY-P7126 Adiponectin/Acrp30 Protein, Human (CHO) Q15848 (E19-N244) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P7127 Adiponectin/Acrp30 Protein, Human (HEK293) Q15848 (K101-N244) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P70504 Adiponectin/Acrp30 Protein, Human (HEK293, His) Q15848 (E19-N244) ≥ 95%, as determined by reducing SDS-PAGE.

ADIPOQ Antibodies

Cat. No. Product Name Application Reactivity
HY-P86517 Adiponectin Antibody (YA6209) WB, IHC-P, ICC/IF, IP, ELISA Human, Mouse, Rat

Related Diseases

Diseases Alias
Adiponectin, Serum Level Of, Quantitative Trait Locus 1
  • Adiponectin Deficiency

  • ADIPQTL1

  • ADPND

Fatty Liver Disease
  • Alcoholic Fatty Liver

  • Fatty Liver

  • Fatty Liver, Alcoholic

  • Fatty Change Of Liver

  • Hepatic Lipidosis

  • Steatosis Of Liver

  • Fatty Liver Alcoholic

  • Steatohepatitis

  • Etoh Fatty Liver

  • Etoh Fatty Liver Metamorphosis

  • Fatty Etoh Liver Necrosis

Prediabetes Syndrome
  • Prediabetes

  • Impaired Glucose Tolerance

  • Prediabetic State

  • IGT

  • Igt - [Impaired Glucose Tolerance]

  • Impaired Glucose Tolerance With Unspecified Complication

  • Impaired Glucose Tolerance Without Complication

  • Abnormal Glucose Tolerance

Glucose Intolerance
  • Glucose: Intolerance

  • Glucose: Malabsorption

  • Malabsorption Of Glucose

  • Impaired Glucose Tolerance

Gestational Diabetes
  • Gestational Diabetes Mellitus

  • GDM

  • Diabetes Mellitus Arising In Pregnancy

  • Maternal Gestational Diabetes Mellitus

  • Diabetes Mellitus, Gestational

  • Diabetes Mellitus, Pregnancy Related

  • Diabetes, Pregnancy-Induced

  • Diabetes Gestational

  • Diabetes, Gestational

  • Diabetes Of Pregnancy

  • Gdm - [Gestational Diabetes Mellitus]

  • Gestational Diabetes Mellitus Nos

  • Gestational Diabetes Complicating Pregnancy, Childbirth, Or The Puerperium

Liver Disease
  • Liver Failure

  • Liver Diseases

  • Abnormality Of The Liver

  • Liver Dysfunction

  • Disorder Of Liver

  • Hepatic Disorder

  • Hepatic Disease

  • Disease Of Bilirubin Metabolism

  • Disorder Of Bilirubin Metabolism

  • Liver Decompensation

  • Liver Function Failure

  • Hepatic Failure Nos

  • Liver Failure Nos

  • End Stage Liver Disease

  • Decompensated Liver Failure

  • Decompensation Of Liver Function

  • Hepatic Decompensation

  • Hepatic Insufficiency

  • Liver Cell Necrosis With Hepatic Failure

  • Liver Insufficiency

  • Decompensated Liver Disease

  • End Stage Liver Failure

  • Liver Necrosis With Hepatic Failure

Acquired Generalized Lipodystrophy
  • Lawrence Syndrome

  • Acquired Lipoatrophic Diabetes

  • Lawrence-Seip Syndrome

  • Familial Generalized Lipodystrophy

Hyperglycemia
Obesity-Hypoventilation Syndrome
  • Obesity Hypoventilation Syndrome

  • Pickwickian Syndrome

  • Cardiopulmonary Obesity Syndrome

  • Extreme Obesity With Alveolar Hypoventilation With Body-Mass-Index Unspecified

  • Alveolar Hypoventilation Syndrome

  • Alveolus Hypoventilation Syndrome

  • Ohs - [Obesity Hypoventilation Syndrome]

Arteriolosclerosis
Leptin Deficiency Or Dysfunction
  • Morbid Obesity

  • Obesity Due To Congenital Leptin Deficiency

  • LEPD

  • Congenital Leptin Deficiency

  • Obesity, Morbid

  • Obesity, Morbid, Due To Leptin Deficiency

  • Severe Obesity

  • Obesity, Morbid, Nonsyndromic 1

  • Leptin Deficiency

  • Obesity, Severe, Due To Leptin Deficiency

  • Leptin

  • Morbid Obesity Due To Leptin Deficiency

  • Obesity Morbid

  • Leptin Dysfunction

Diabetes Mellitus
  • Diabetes

Acanthosis Nigricans
  • Keratosis Nigricans

  • An

Anorexia Nervosa
  • Anorexia Nervosa, Susceptibility To

  • ANON

  • Anorexia Nervosa, Susceptibility To, 1

  • An

  • Anorexia Nervosa 1

  • An - [Anorexia Nervosa]

Arteriosclerosis Obliterans
Apnea, Obstructive Sleep
  • Obstructive Sleep Apnea Syndrome

  • Obstructive Sleep Apnea

  • Sleep Apnea, Obstructive

  • Osa

  • Osas

  • Sleep Apnea/Hypopnea Syndrome

  • Sahs

  • Upper Airway Resistance Sleep Apnea Syndrome

  • Apnea, Obstructive

  • Obstructive Apnea

  • Osahs

  • Sleep Apnea Hypopnea Syndrome

  • Sleep Apnea Syndrome, Obstructive

  • Sleep Apnea Obstructive

  • Sleep Apnea Syndromes

  • Obstructive Sleep Apnoea Syndrome

  • Obstructive Sleep Apnoea, Adult

  • Osa - [Obstructive Sleep Apnoea]

  • Obstructive Sleep Apnoea, Paediatric

  • Obstructive Sleep Apnoea Hypopnoea Syndrome

  • Osa Syndrome

  • Sleep Apnoea Nos

  • [Sas] - Sleep Apnoea Syndrome

  • Sleep Apnoea Syndrome

  • [Osahs] - Obstructive Sleep Apnoea-Hypopnea Syndrome

  • [Sahs] - Sleep Apnoea-Hypopnea Syndrome

Arteriosclerosis
  • Arteriosclerotic Vascular Disease

Abdominal Obesity-Metabolic Syndrome 1
  • Metabolic Syndrome X

  • Metabolic Syndrome

  • AOMS1

  • Dysmetabolic Syndrome X

  • Metabolic Disease

  • Abdominal Obesity Metabolic Syndrome

Type 2 Diabetes Mellitus
  • Insulin Resistance

  • NIDDM

  • Type 2 Diabetes

  • Diabetes Mellitus, Non-Insulin-Dependent

  • T2D

  • Noninsulin-Dependent Diabetes Mellitus

  • Diabetes Mellitus, Type Ii

  • Maturity-Onset Diabetes

  • Insulin Resistance, Severe, Digenic

  • Diabetes Mellitus, Type 2

  • Diabetes Mellitus, Noninsulin-Dependent

  • Diabetes Mellitus, Noninsulin-Dependent, Association With

  • Diabetes Mellitus, Noninsulin-Dependent, Late Onset

  • Hypertension, Insulin Resistance-Related, Susceptibility To

  • Insulin Resistance, Susceptibility To

  • Non-Insulin-Dependent Diabetes Mellitus

  • Type Ii Diabetes Mellitus

  • Adult-Onset Diabetes Mellitus

  • Maturity-Onset Diabetes Mellitus

  • Diabetes Mellitus Type 2

  • Type Ii Diabetes

  • Type 2 Diabetes Mellitus, Susceptibility To

  • Diabetes, Type 2

  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To

  • Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To

  • Diabetes Mellitus, Type 2, Susceptibility To

  • Diabetes Mellitus, Noninsulin-Dependent, 2

  • Diabetes Mellitus, Type Ii, Susceptibility To

  • Hypertension, Insulin Resistance-Related

  • Adult-Onset Diabetes

  • Aodm

  • Diabetes Mellitus, Adult-Onset

  • Diabetes Mellitus Type Ii

  • Diabetes Mellitus Type 2, Susceptibility To

  • Diabetes, Type Ii, Susceptibility To

  • Diabetes Type 2

  • Diabetes Mellitus

  • Adult Onset Diabetes

  • Maturity Onset Diabetes

  • Nonketotic Diabetes

  • Non-Insulin Dependent Diabetes Mellitus

  • T2dm - [Type 2 Diabetes Mellitus]

  • Niddm - [Non Insulin Dependent Diabetes Mellitus]

  • Dm2

  • Dm Type Ii

  • Diabetic Type 2

  • Insulin Requiring Type 2 Diabetes

  • Noninsulin Dependent Diabetes

  • Non-Insulin-Dependent Diabetes Mellitus Without Complications

  • Diabetes Due To Insulin Secretory Defect

  • Diabetes Mellitus Due To Insulin Secretory Defect

  • Non-Insulin-Dependent Diabetes Of The Young

  • Senile Diabetes

  • Nonketotic Hyperglycaemia

  • Stable Diabetes

Lipid Metabolism Disorder
  • Dyslipidemia

  • Disorder Of Fatty Acid Metabolism

  • Lipid Metabolism Disorders

  • Fatty Acid Metabolism Disorder

  • Disorder Of Lipid Metabolism

  • Abnormality Of Lipid Metabolism

  • Lipid Metabolism, Inborn Errors

  • Dyslipidemias

  • Disorders Of Lipid Metabolism

  • Congenital Disorders Of Lipid Metabolism

  • Inherited Disorders Of Lipid Metabolism

Proteasome-Associated Autoinflammatory Syndrome 1
  • Jmp Syndrome

  • Nakajo-Nishimura Syndrome

  • Nkjo

  • Autoinflammation, Lipodystrophy, And Dermatosis Syndrome

  • Proteasome-Associated Autoinflammatory Syndrome 1 And Digenic Forms

  • Nakajo Syndrome

  • PRAAS1

  • Chronic Atypical Neutrophilic Dermatosis With Lipodystrophy And Elevated Temperature Syndrome

  • Candle

  • Joint Contractures, Muscular Atrophy, Microcytic Anemia, And Panniculitis-Induced Lipodystrophy

  • Aldd

  • Inflammation

  • Joint Contractures - Muscle Atrophy - Microcytic Anemia - Panniculitis-Induced Lipodystrophy

  • Nakajo Nishimura Syndrome

  • Amyotrophy Fat Tissue Anomaly

  • Japanese Autoinflammatory Syndrome With Lipodystrophy

  • Jasl

  • Joint Contractures Muscular Atrophy Microcytic Anemia And Panniculitis-Induced Lipodystrophy

  • Nns

  • Nodular Erythema With Digital Changes

  • Secondary Hypertrophic Osteoperiostosis With Pernio

Sleep Apnea
  • Sleep Apnea Syndromes

Hyperandrogenism
  • Hyperandrogenization Syndrome

Non-Alcoholic Fatty Liver Disease
  • Fatty Liver

  • Non-Alcoholic Fatty Liver

  • Nafld

  • Nonalcoholic Fatty Liver Disease

  • Nonalcoholic Steatohepatitis

  • Steatosis

  • Nafl

  • Nash

  • Non-Alcoholic Steatohepatitis

  • Susceptibility To Nonalcoholic Fatty Liver Disease

  • Steatohepatitis

  • Fatty Degeneration

  • Non-Alcoholic Fatty Liver Disease Without Mention Of Non-Alcoholic Steatohepatitis

  • Nafld Without Nash

  • Nafld Without Mention Of Nash

Polycystic Ovary Syndrome
  • Polycystic Ovarian Syndrome

  • Pcos

  • Polycystic Ovarian Disease

  • Polycystic Ovaries

  • Stein-Leventhal Syndrome

  • Multicystic Ovaries

  • Polycystic Ovary

  • Sclerocystic Ovaries

  • Sclerocystic Ovary Syndrome

  • Stein-Leventhal Synd.

  • Cystic Disease Of Ovaries

  • Cystic Disease Of Ovary

  • Pco

  • Pcod

  • Sclerocystic Ovarian Degeneration

  • Polycystic Ovary Syndrome, Susceptibility To

  • Pcos - [Polycystic Ovary Syndrome]

  • Polycystic Ovary Nos

  • Pco - [Polycystic Ovary]

Cardiovascular System Disease
  • Abnormality Of The Cardiovascular System

  • Cardiovascular Disease

  • Disease Of Subdivision Of Hemolymphoid System

  • Disorder Of Cardiovascular System

  • Cardiovascular Diseases

Severe Pre-Eclampsia
  • Severe Preeclampsia

  • Antepartum Severe Pre-Eclampsia

  • Postpartum Severe Pre-Eclampsia

  • Severe Pre-Eclampsia, With Delivery

  • Severe Toxemia

  • Severe Pre-Eclampsia, Antepartum Condition Or Complication

  • Severe Pre-Eclampsia, Postpartum Condition Or Complication

  • Severe Puerperal Pre-Eclampsia

  • Severe Pre-Eclamptic Toxaemia

  • Severe Pet - [Pre-Eclamptic Toxaemia]

Vascular Disease
  • Vascular Diseases

  • Aneurysm

  • Spinal Cord Ischemia

  • Vascular Anomaly

  • Spinal Cord Vascular Diseases

  • Vascular Tissue Disease

Laron Syndrome
  • Growth Hormone Insensitivity Syndrome

  • Growth Hormone Receptor Deficiency

  • Laron Dwarfism

  • Pituitary Dwarfism Ii

  • Laron-Type Isolated Somatotropin Defect

  • Primary Growth Hormone Resistance

  • Laron-Type Dwarfism

  • Laron Type Pituitary Dwarfism I

  • Primary Growth Hormone Insensitivity

  • Primary Gh Resistance

  • Gh-R Deficiency

  • Growth Hormone Receptor Defect

  • Laron-Type Pituitary Dwarfism

  • Laron-Type Short Stature

  • Severe Gh Insensitivity

  • Ghis

  • Short Stature Due To A Defect In Growth Hormone Receptor Or Post-Receptor Pathway

  • Complete Growth Hormone Insensitivity

  • Gh Receptor Deficiency

  • Primary Gh Insensitivity

  • Short Stature Due To Growth Hormone Resistance

  • LARS

Atherosclerosis Susceptibility
  • Atherosclerosis

  • Atherosclerosis, Susceptibility To

  • ATHS

  • Atherogenic Lipoprotein Phenotype

  • Alp

  • Arteriosclerosis

Chronic Kidney Disease
  • Chronic Renal Disease

  • Chronic Kidney Failure

  • Ckd

  • Chronic Renal Failure

  • Kidney Failure, Chronic

  • Chronic Renal Failure Syndrome

  • Crf

  • Renal Failure - Chronic

  • Renal Failure Chronic

  • Chronic Kidney Diseases

  • Chronic Kidney Disease Stage 5

  • Ckd - [Chronic Kidney Disease]

  • Crf - [Chronic Renal Failure]

  • Chronic Kidney Impairment

  • Chronic Renal Impairment

  • Chronic Kidney Shutdown

  • Chronic Hypoxic Kidney Failure

  • Chronic Kidney Collapse

  • Chronic Renal Insufficiency

  • Chronic Kidney Toxaemia

  • Chronic Kidney Hypofunction

  • Chronic Renal Suppression

  • Chronic Renal Failure, Stage 5

  • Ckd - [Chronic Kidney Disease] Stage 5

  • End Stage Kidney Failure

  • End Stage Renal Failure

  • End Stage Kidney Disease

  • End Stage Renal Disease

  • End Stage Chronic Renal Failure

  • Esrf - [End Stage Renal Failure]

  • Esrd - [End Stage Renal Diseases]

  • Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²

Liver Cirrhosis
  • Cirrhosis

  • Cirrhosis Of Liver

  • CIRRH

  • Cryptogenic Cirrhosis

  • Cirrhosis, Cryptogenic

  • Cirrhosis Nos

Mandibular Hypoplasia, Deafness, Progeroid Features, And Lipodystrophy Syndrome
  • Mdp Syndrome

  • Mandibular Hypoplasia-Deafness-Progeroid Syndrome

  • MDPL

  • Mdpl Syndrome

  • Mandibular Hypoplasia-Deafness-Progeroid Features-Lipodystrophy Syndrome

  • Mandibular Hypoplasia-Hearing Loss-Progeroid Syndrome

  • Lipodystrophy

  • Mandibular Hypoplasia, Deafness, Progeroid Features

  • Hypoplasia, Mandibular, Deafness, Progeroid Features, And Lipodystrophy Syndrome

  • Andibular Hypoplasia, Deafness, Progeroid Features, And Lipodystrophy Syndrome

Hyperinsulinism
  • Hyperinsulinemia

Acquired Metabolic Disease
Prader-Willi Syndrome
  • Prader-Labhart-Willi Syndrome

  • PWS

  • Willi-Prader Syndrome

  • Prader-Willi Syndrome Due To Translocation

  • Prader-Willi Syndrome Due To Imprinting Mutation

  • Prader-Willi Syndrome Due To Maternal Uniparental Disomy Of Chromosome 15

  • Prader Willi Syndrome

  • Upd(15)Mat

Pre-Eclampsia
  • Preeclampsia

  • Gestational Hypertension

  • Hypertension Induced By Pregnancy

  • Pre-Eclamptic Toxaemia

  • Pregnancy Associated Hypertension

  • Proteinuric Hypertension Of Pregnancy

  • Hypertension, Pregnancy-Induced, Susceptibility To

  • Preeclampsia/Eclampsia

  • Pregnancy Toxemia

  • Toxaemia Of Pregnancy

  • Gestational Proteinuric Hypertension

  • Pregnancy-Induced Hypertension

  • Toxemia Of Pregnancy

  • Preeclampsia, Susceptibility To

  • Transient Hypertension Of Pregnancy

  • Gestational [Pregnancy-Induced] Hypertension Without Significant Proteinuria

  • Gestational Hypertension Nos

  • Mild Proteinuric Hypertension Of Pregnancy

  • Pih - [Pregnancy-Induced Hypertension]

  • Pregnancy-Induced Hypertension Nos

  • Gestational [Pregnancy-Induced] Hypertension With Significant Proteinuria

  • Pe - [Pre-Eclampsia]

  • Pre-Eclampsia Nos

  • Pre-Eclamptic Nos

  • Pregnancy Pre-Eclampsia

  • Puerperal Pre-Eclampsia

  • Pre-Eclampsia Toxaemia

  • Toxaemia In Pregnancy

  • Pet - [Pre-Eclamptic Toxaemia]

  • Maternal Toxaemia

Lipodystrophy, Familial Partial, Type 2
  • FPLD2

  • Lipoatrophic Diabetes

  • Familial Partial Lipodystrophy Type 2

  • Familial Partial Lipodystrophy, Dunnigan Type

  • Fpl2

  • Lipoatrophic Diabetes Mellitus

  • Lipodystrophy, Familial Partial, Dunnigan Type

  • Lipodystrophy, Familial, Of Limbs And Lower Trunk

  • Lipodystrophy, Reverse Partial

  • Familial Partial Lipodystrophy Dunnigan Type

  • Dunnigan Syndrome

  • Familial Lipodystrophy Of Limbs And Lower Trunk

  • Reverse Partial Lipodystrophy

  • Lipodystrophy, Familial Partial, 2

  • Generalized Lipoatrophy Associated With Diabetes, Hepatic Steatosis, Hypertrophic Cardiomyopathy And Leukomelanodermic Papules

  • Lipodystrophy Familial Of Limbs And Lower Trunk

  • Lipodystrophy Reverse Partial

  • Diabetes Mellitus, Lipoatrophic

  • Familial Partial Lipodystrophy, Type 2

  • Familial Generalized Lipodystrophy

Heart Disease
  • Heart Failure

  • Congenital Heart Disease

  • Heart Diseases

  • Congenital Heart Defects

  • Congenital Heart Defect

  • Heart Malformation

  • Congenital Anomaly Of Heart

  • Heart Defect

  • Heart-Congenital Defect

  • Congenital Heart Disorder

  • Heart Defects Congenital

  • Heart Defects, Congenital

  • Heart Defects

  • Heart Disease, Congenital

  • Disease, Heart, Congenital

  • Congestive Heart Failure

Familial Partial Lipodystrophy
  • Lipodystrophy, Familial Partial

  • Fpld

  • Kobberling-Dunnigan Syndrome

  • Dunnigan Syndrome

  • Koberling-Dunnigan Syndrome

  • Dunnigan-Kobberling Syndrome

  • Fpl

  • Familial Partial Lipodystrophy, Type 2

Body Mass Index Quantitative Trait Locus 11
  • OBESITY

  • Obesity, Susceptibility To

  • Leanness, Inherited

  • Obesity, Susceptibility To, Bmiq11

  • Obesity, Mild, Early-Onset

  • Obesity, Association With

  • Obesity, Early-Onset, Susceptibility To

  • Obesity, Severe

  • Obesity, Severe, And Type Ii Diabetes

  • Obesity, Late-Onset

  • Obesity , Susceptibility To

  • BMIQ11

  • Obesity Bmiq11

  • Obesity, Early-Onset

  • Simple Obesity Nos

  • Excess Fat

  • Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified

  • Adiposis

Pericarditis
Acromegaly
  • Gigantism

  • Growth Hormone Excess

  • Pituitary Giant

  • Somatotroph Adenoma

  • Growth Hormone-Secreting Pituitary Adenoma

Overnutrition
Familial Hyperlipidemia
  • Familial Hyperlipoproteinemia

  • Hyperlipidaemia

  • Hyperlipoproteinemias

  • Hyperlipidemia

  • Hyperlipemia

  • Hyperlipidemias

Hypertension, Essential
  • Essential Hypertension

  • Hypertension

  • High Blood Pressure

  • Hypertension, Essential, Susceptibility To

  • Hypertensive Disease

  • Primary Hypertension

  • EHT

  • Hypertension, Salt-Sensitive Essential, Susceptibility To

  • Hyperpiesia

  • Idiopathic Hypertension

  • Hypertensive Disorder

  • Hypertension, Essential, Susceptibility To, 3

  • Hypertension, Essential 3

  • Hypertension, Essential, Salt-Sensitive

  • Hypertension, Essential, Susceptibility To, 6

  • Hypertension, Essential 6

  • Hypertension, Salt-Sensitive Essential

  • Hypertension, Susceptibility To

  • Hypertension, Essential, Susceptibility To, 4

  • Hypertension, Essential 4

  • Hypertension, Essential, Susceptibility To, 2

  • Hypertension, Essential 2

  • Hypertension, Essential, Susceptibility To, 1

  • Hypertension, Essential 1

  • Hypertension, Essential, Susceptibility To, 5

  • Hypertension, Essential 5

  • Htn

  • Vascular Hypertensive Disorder

  • Systemic Primary Arterial Hypertension

  • Hbp - [High Blood Pressure]

  • Systemic Arterial Hypertensive Disorder

  • Elevated Blood Pressure

  • Arterial Hypertension Nos

  • Hypertension Nos

  • Benign Hypertension

  • Systemic Arterial Hypertension

  • Systemic Hypertension

  • Artery Htn

  • Benign Htn

  • Vascular Htn

  • Vascular Hypertension

  • Cholesterol Hypertension

  • Cholesterol Htn

  • Idiopathic Htn

  • Malignant Hypertension

  • Malignant Htn

  • Raised Blood Pressure

  • Cardiovascular Hypertension

  • Primary Htn - [Hypertension]

  • High Arterial Tension

  • High Blood Pressure Disorder

  • Ht - [Hypertension]

  • Htn - [Hypertension]

  • Hypertensive Vascular Disease

  • Hypertensive Vascular Degeneration

Congenital Generalized Lipodystrophy
  • Berardinelli-Seip Congenital Lipodystrophy

  • Berardinelli-Seip Syndrome

  • Brunzell Syndrome

  • Bscl

  • Generalized Lipodystrophy

  • Lipodystrophy, Congenital Generalized

  • Seip Syndrome

  • Total Lipodystrophy

  • Cgl

  • Lipoatrophic Diabetes

  • Lipodystrophy, Generalized, Congenital

  • Familial Generalized Lipodystrophy

  • Congenital Generalized Lipodystrophy Type 2

  • Lipoatrophic Diabetes Mellitus

  • Familial Partial Lipodystrophy, Type 2

Pellagra
  • Niacin Deficiency

  • Niacin-Tryptophan Deficiency

  • Pellagroid Syndrome

Carotid Stenosis
  • Carotid Artery Stenosis

  • Stenosis, Carotid Artery

Kidney Disease
  • Renal Failure

  • Kidney Failure

  • Kidney Diseases

  • Nephropathy

  • Abnormality Of The Kidney

  • Impaired Renal Function Disease

  • Renal Anomaly

  • Kidney Dysfunction

  • Renal Disease

  • Nephropathies

  • Renal Failure Adverse Event

  • Abnormal Renal Function

Calcification Of Joints And Arteries
  • Hereditary Arterial And Articular Multiple Calcification Syndrome

  • CALJA

  • Arterial Calcification Due To Cd73 Deficiency

  • Arterial Calcification Due To Deficiency Of Cd73

  • Acdc

  • Arterial Calcification And Distal Joint Calcification

  • Arterial Calcification Due To Deficiency Of Cd73:Acdc

  • Calcification Of Joints And Arteries

  • Calja

Hyperlipidemia, Familial Combined, 3
  • Familial Combined Hyperlipidemia

  • Combined Hyperlipidemia, Familial

  • Mixed Hyperlipidaemia

  • FCHL3

  • Hyperlipidemia, Familial Combined

  • Familial Multiple Lipoprotein-Type Hyperlipidemia

  • Hyperbetalipoproteinemia With Prebetalipoproteinemia

  • Type Iib Hyperlipoproteinemia

  • Hyperlipidemia Familial Combined

  • Hyperlipoproteinemia Type Iib

  • Mixed Hyperlipemia

  • Hyperlipidaemia, Group C

  • Familial Hypercholesterolaemia With Hyperlipaemia

  • Familial Hyperbetalipoproteinaemia And Hyperprebetalipoproteinaemia

  • Hyperbetalipoproteinaemia With Prebetalipoproteinaemia

  • Hypercholesterolaemia With Endogenous Hyperglyceridaemia

  • Prebetalipoproteinemia Hyperbetalipoproteinaemia

  • Remnant Hyperlipoproteinemia

Lipoprotein Quantitative Trait Locus
  • Coronary Artery Disease

  • Coronary Artery Anomaly

  • Coronary Artery Disease, Susceptibility To

  • Myocardial Ischemia

  • Congenital Anomaly Of Coronary Artery

  • Coronary Arteriosclerosis

  • Coronary Disease

  • Coronary Heart Disease

  • Coronary Artery Disorder

  • LPAQTL

  • Lpa Deficiency, Congenital

  • Coronary Artery Abnormality

  • Coronary Artery Anomaly, Congenital

  • Chd

  • Coronary Syndrome

  • Congenital Malformations Of Coronary Vessels

  • Malformation Of Coronary Vessels

  • Congenital Coronary Artery Anomaly

  • Congenital Coronary Artery Deformity

  • Congenital Coronary Artery Disorder

  • Abnormal Coronary Artery

  • Congenital Coronary Artery Malposition

  • Congenital Coronary Disease

  • Congenital Anomaly Of Coronary Arteries

Gastroesophageal Reflux
  • Gastroesophageal Reflux Disease

  • Gerd

  • GER

  • Gastroesophageal Reflux, Pediatric

  • Acid Reflux

  • Gastresophageal Reflux

  • Gastro-Esophageal Reflux

  • Gerd - Gastro-Esophageal Reflux Disease

Hypothyroidism
  • Thyroid Diseases

  • Thyroid Disease

  • Thyroid Deficiency

  • Thyroid Insufficiency

  • Dysfunction Thyroid

  • Thyroid Dysfunction

Hutchinson-Gilford Progeria Syndrome
  • Progeria

  • HGPS

  • Hutchinson-Gilford Syndrome

  • Hutchinson-Gilford Progeria

  • Hutchinson Gilford Syndrome

  • Hutchinson Gilford Progeria Syndrome

  • Hutchinson-Gilford Disease

  • Progeria Of Childhood

  • Hutchinson-Gilford-Progeria Syndrome

Hyperthyroidism
  • Overactive Thyroid

Nutritional Deficiency Disease
  • Malnutrition

  • Nutritional Disorder

  • Nutritional Deficiency

  • Nutrition

  • Deficiency Diseases

  • Carbamoyl-Phosphate Synthase I Deficiency Disease

  • Nutrition Disorders

Myocardial Infarction
  • Heart Attack

  • Myocardial Infarction, Susceptibility To

  • Myocardial Infarction 1

  • Myocardial Infarction, Protection Against

  • Myocardial Infarction, Decreased Susceptibility To

  • Myocardial Infarction, Decreased

  • Myocardial Infarct

  • MCI1

  • Premature Myocardial Infarction

  • Myocardial Infarction, Susceptibility To, Type 1

Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2
  • Abdominal Obesity-Metabolic Syndrome

  • Abdominal Obesity Metabolic Syndrome

  • Metabolic Syndrome X

  • Aoms2

  • Aoms1

Lipid Storage Disease
  • Lipoidosis

  • Inborn Lipid Storage Disorder

  • Lipoid Storage Diseas

  • Lipid Storage Diseases

  • Lipidoses

Ovarian Disease
  • Ovarian Dysfunction

  • Ovarian Diseases

  • Ovarian Disorders

  • Disorder Of Endocrine Ovary

Non-Alcoholic Steatohepatitis
  • Nonalcoholic Steatohepatitis

  • Nash

  • Nash - [Non-Alcoholic Steatohepatitis]

  • Non-Alcoholic Steatohepatosis

Conn'S Syndrome
  • Cushing Syndrome

  • Hyperaldosteronism

  • Primary Hyperaldosteronism

  • Hypercortisolism

  • Primary Aldosteronism

  • Cushing'S Syndrome

  • Adrenal Gland Hyperfunction

  • Conn Syndrome

  • Hyperadrenalism

  • Ectopic Acth Syndrome

  • Hyperadrenocorticism

  • Cushing Disease

  • Cushing'S Disease

  • Adrenal Cortex Adenoma

  • Corticotroph Pituitary Adenoma

  • Pituitary Corticotroph Micro-Adenoma

  • Pituitary-Dependent Cushing Syndrome

  • Pituitary Acth Hypersecretion

  • Acth Syndrome, Ectopic

  • Acth-Secreting Pituitary Adenoma

  • Adrenal Hyperfunction Resulting From Pituitary Acth Excess

  • Ectopic Adrenocorticotropic Hormone Syndrome

  • Nodular Primary Adrenocortical Dysplasia

  • Pituitary Dependent Cushing Syndrome

  • Pituitary Cushing Syndrome

  • Pituitary-Dependant Cushing Syndrome

  • Pituitary-Dependant Hypercortisolism

  • Pituitary-Dependant Hypercortisolism Disorder

  • Aldosteronism Primary

  • Acth Syndrome Ectopic

  • Adrenal Cushing'S Syndrome

  • Adrenal Cortical Adenoma

  • Cushing Syndrome Nos

  • Cortisol Hypersecretion

  • Corticoadrenal Hypersecretion

  • Cushing Syndrome Secondary To Ectopic Acth-Secretion

  • Ectopic Cushing Syndrome

  • Hypercortisolism Due To Nonpituitary Tumour

  • Ectopic Acth - [Adrenocorticotropic Hormone] Secretion

  • Ectopic Acth - [Adrenocorticotropic Hormone] Secretion Causing Cushing Syndrome

  • Idiopathic Aldosteronism

  • Aldosteronism

  • Primary Aldosteronism Due To Bilateral Adrenal Hyperplasia

  • Primary Aldosteronism Due To Adrenal Hyperplasia

Carbohydrate Metabolic Disorder
  • Inborn Errors Of Carbohydrate Metabolism

  • Disorder Of Carbohydrate Metabolism

  • Carbohydrate Metabolism, Inborn Errors

  • Disorder Of Carbohydrate Transport And Metabolism

  • Inborn Carbohydrate Metabolism Disorder

  • Inborn Carbohydrate Metabolic Disorder

  • Carbohydrate Metabolism Disorder

  • Carbohydrate Metabolism Disorders

  • Disorders Of Carbohydrate Metabolism

  • Congenital Disorders Of Carbohydrate Metabolism

  • Inherited Disorders Of Carbohydrate Metabolism

Glucose Metabolism Disease
  • Glucose Metabolism Disorders

  • Disorder Of Glucose Metabolism

Nonobstructive Coronary Artery Disease
  • Non-Cad

  • Non-Obstructive Coronary Artery Disease

Adult Syndrome
  • Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome

  • Acro Dermato Ungual Lacrimal Tooth Syndrome

  • Pigment Anomaly-Ectrodactyly-Hypodontia Syndrome

  • Acro-Dermato-Ungual-Lacrimal-Tooth Syndrome

  • Adult

Asthma
  • Chronic Obstructive Asthma

  • Asthma, Diminished Response To Antileukotriene Treatment In

  • Bronchial Hyperreactivity

  • Asthma, Susceptibility To

  • Asthma, Bronchial

  • Asthma, Protection Against

  • Asthma, Nocturnal, Susceptibility To

  • Nocturnal Asthma

  • Asthma-Related Traits

  • Asthma-Related Traits, Susceptibility To

  • Asthma, Nocturnal

  • Chronic Obstructive Asthma With Acute Exacerbation

  • Chronic Obstructive Asthma With Status Asthmaticus

  • Exercise Induced Asthma

  • Exercise-Induced Asthma

  • Bronchial Asthma

  • Asthma, Exercise-Induced

  • Idiosyncratic Asthma

  • Unspecified Asthma With Acute Exacerbation

  • Asthma, Unspecified, With Stated Status Asthmaticus

  • Status Asthmaticus Nos

  • Acute Severe Asthma

  • Acute Severe Bronchial Asthma

  • Status Asthma

  • Status Post Asthmaticus

Hypoglycemia
  • Hypoglycaemia

  • Low Blood Sugar

  • Hypoglycaemia Nos

  • Spontaneous Hypoglycaemia

  • Nondiabetic Hypoglycaemia

  • Hypoglycaemic Disorder Nos

  • Hypoglycaemic Syndrome

Prolactinoma
  • Prolactin-Producing Pituitary Gland Adenoma

  • Prolactin-Secreting Pituitary Adenoma

  • Forbes-Albright Syndrome

  • Lactotroph Adenoma

  • Prl-Secreting Pituitary Adenoma

  • Prloma

  • Pituitary Lactotrophic Adenoma

  • Familial Prolactinoma

  • Pituitary Adenoma, Prolactin-Secreting

  • Prolactinoma Of Pituitary Gland

  • PSPA

Complete Generalized Lipodystrophy
Inherited Metabolic Disorder
  • Inborn Errors Of Metabolism

  • Inborn Metabolic Disorder

  • Inborn Metabolism Disorder

  • Metabolic Hereditary Disorder

  • Inborn Error Of Metabolism

  • Metabolism, Inborn Errors

Endometrial Cancer
  • Endometrial Carcinoma

  • Endometrial Neoplasm

  • Malignant Neoplasm Of Endometrium

  • Endometrioid Carcinoma

  • Endometrial Neoplasms

  • Carcinoma, Endometrioid

  • Endometrial Cancer, Familial

  • Endometrial Carcinoma, Somatic

  • Endometrial Cancer, Susceptibility To

  • Endometrial Ca

  • Malignant Endometrial Neoplasm

  • Neoplasm Of Endometrium

  • Primary Malignant Neoplasm Of Endometrium

  • Tumor Of Endometrium

  • Carcinoma Of The Endometrium

  • Endometrioid Carcinoma Of Female Reproductive System

  • ENDMC

  • Carcinoma Endometrioid

  • Endometrial Cancers

  • Cancer, Endometrial

  • Uterine Corpus Cancer

Coronary Heart Disease 1
  • Coronary Heart Disease

  • Coronary Heart Disease, Susceptibility To, 1

  • Chds1

  • Coronary Heart Disease, Susceptibility To

  • CHD

  • Heart, Coronary, Disease, Susceptibility To, Type 1

  • Coronary Arteriosclerosis

  • Coronary Artery Disease

Osteoporosis
  • Postmenopausal Osteoporosis

  • Osteoporosis, Postmenopausal

  • Bone Mineral Density Quantitative Trait Locus

  • Bmnd

  • Osteoporosis, Involutional

  • Osteoporosis, Susceptibility To

  • Osteoporosis, Postmenopausal, Susceptibility

  • Bone Mineral Density Variation Qtl, Osteoporosis

  • OSTEOP

  • Involutional Osteoporosis

  • Senile Osteoporosis

  • Osteoporosis Postmenopausal

  • Bone Mineral Density, Quantitative Trait Locus

  • Osteoporosis, Senile

  • Idiopathic Osteoporosis

  • Bone Rarefaction Nos

  • Type 1 Osteoporosis

Lipodystrophy, Congenital Generalized, Type 2
  • Congenital Generalized Lipodystrophy Type 2

  • CGL2

  • Berardinelli-Seip Congenital Lipodystrophy Type 2

  • Berardinelli-Seip Syndrome

  • Brunzell Syndrome Bscl2-Related

  • Total Lipodystrophy And Acromegaloid Gigantism

  • Berardinelli-Seip Congenital Lipodystrophy, Type 2

  • Seip Syndrome

  • Berardinelli Syndrome

  • Lipodystrophy, Total, And Acromegaloid Gigantism

  • Lipoatrophic Diabetes, Congenital

  • Lipodystrophy, Berardinelli-Seip Congenital, Type 2

  • Brunzell Syndrome, Bscl2-Related

  • Congenital Lipoatrophic Diabetes

  • Congenital Generalized Lipodystrophy 2

  • Lipoatrophic Diabetes

  • Lipodystrophy Berardinelli Type

  • Familial Generalized Lipodystrophy

  • Lipoatrophic Diabetes Mellitus

  • Familial Partial Lipodystrophy, Type 2

Tetralogy Of Fallot
  • TOF

  • Fallot Tetralogy

  • Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle

  • Tetrad Of Fallot

  • Fallot Tetrad

  • Fallot Disease

  • Fallot Complex

  • Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy

  • Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle

  • Interventricular Septal Defect, In Tetralogy Of Fallot

  • Ventricular Septal Defect With Obstructed Right Ventricular Outflow

  • Tof - [Tetralogy Of Fallot]

  • Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]

  • Pulmonary Atresia, Ventricular Septal Defect And Mapcas

  • Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]

Placenta Disease
  • Placenta Diseases

  • Placenta Disorder

  • Pregnancy Complications

  • Placenta Disorders

Sleep Disorder
  • Sleep Disorders

  • Non-Organic Sleep Disorder

Rheumatoid Arthritis
  • RA

  • Arthritis, Rheumatoid

  • Rheumatoid Arthritis, Susceptibility To

  • Arthritis Or Polyarthritis, Rheumatic

  • Atrophic Arthritis

  • Rheumatism Arthritis

  • Rheumatoid Polyarthritis

Arterial Calcification Of Infancy
  • Idiopathic Infantile Arterial Calcification

  • Generalized Arterial Calcification Of Infancy

  • Iiac

  • Occlusive Infantile Arteriopathy

  • Infantile Arteriosclerosis

  • Gaci

  • Idiopathic Obliterative Arteriopathy

  • Generalized Arterial Calcification In Infancy

  • Arteriopathia Calcificans Infantum

  • Diffuse Arterial Calcifying Elastopathy Of Infancy

  • Infantile Calcifying Arteriopathy

  • Medial Coronary Sclerosis Of Infancy

  • Coronary Sclerosis, Medial, Of Infancy

  • Calcification, Arterial, Generalized, Infancy

Lysosomal Storage Disease
  • Lysosomal Storage Diseases

  • Disorder Of Lysosomal Enzyme

  • Inborn Lysosomal Enzyme Disorder

  • Lysosomal Storage Metabolism Disorder

  • Lysosomal Storage Disorder

Generalized Atherosclerosis
  • Generalised Atherosclerosis

Aromatase Excess Syndrome
  • AEXS

  • Increased Aromatase Activity

  • Familial Hyperestrogenism

  • Hereditary Prepubertal Gynecomastia

  • Aromatase Activity, Increased

  • Familial Gynecomastia Due To Increased Aromatase Activity

  • Hereditary Gynecomastia

  • Gynecomastia, Familial

  • Familial Gynecomastia

Pheochromocytoma
  • Pheochromocytoma, Susceptibility To

  • Phaeochromocytoma

  • Adrenal Gland Chromaffin Paraganglioma

  • Adrenal Gland Chromaffinoma

  • Adrenal Gland Paraganglioma

  • Adrenal Gland Pheochromocytoma

  • Chromaffin Paraganglioma Of The Adrenal Gland

  • Intraadrenal Paraganglioma

  • PCC

  • Chromaffin Cell Tumor

  • Medullary Chromaffinoma

  • Medullary Paraganglioma

  • Pheochromoblastoma

  • Pheochromocytomas

  • Chromaffin Cell Neoplasm

  • Pheochromocytoma, Malignant

Scoliosis
Colorectal Cancer
  • Colon Cancer

  • Colorectal Carcinoma

  • Colon Carcinoma

  • Colorectal Cancer, Susceptibility To

  • Carcinoma Of Colon

  • CRC

  • Colorectal Cancer With Chromosomal Instability, Somatic

  • Colon Cancer, Somatic

  • Colon Cancer, Susceptibility To

  • Colonic Neoplasms

  • Colorectal Neoplasms

  • Colorectal Cancer, Somatic

  • Colon Cancer, Advanced, Somatic

  • Colonic Carcinoma

  • Colorectal Carcinomas

  • Colon Cancers

  • Colorectal Cancers

  • Cancer, Colorectal, Somatic

  • Cancer, Colon

  • Cancer, Colorectal, Susceptibility To

  • Colorectal Neoplasm

  • Colonic Neoplasm

  • Malignant Tumor Of Colon

Psychotic Disorder
  • Psychotic Disorders

  • Mental Or Behavioural Disorder

  • Psychotic

  • Mental Disorders

Arteries, Anomalies Of
  • Artery Disease

  • Arteriopathic Disease

Inflammatory Bowel Disease
  • Inflammatory Bowel Diseases

  • Bowel Disease, Inflammatory

Autism Spectrum Disorder
  • Asd

  • Autism Spectrum Disorders

  • Autistic Continuum

  • Pervasive Developmental Disorder

  • Pervasive Development Disorder

  • Autistic Behavior

  • Autistic Disorder

  • Autistic

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Childhood Autism

  • Kanner Syndrome

  • Pervasive Developmental Delay Nos

  • Pervasive Developmental Disorder, Not Otherwise Specified

Disorder Of Sexual Development
  • Disorder Of Sex Development

  • Disorders Of Sex Development

  • Sex Development Disorder

  • Sex Differentiation Disease

  • Dsd

  • Sex Differentiation Disorders

Schizophrenia
  • SCZD

  • Schizophrenia With Or Without An Affective Disorder

  • Schizophrenia 12

  • Schizophrenia, Susceptibility To

  • Schizophrenia-1

  • Dementia Praecox

  • Schizophrenia 1

Breast Cancer
  • Breast Carcinoma

  • Male Breast Cancer

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation

Autism
  • Autistic Disorder

  • Autism Susceptibility 1

  • Childhood Autism

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Kanner'S Syndrome

  • Autistic

Connective Tissue Disease
  • Connective Tissue Diseases

  • Connective Tissue Disorder

  • Abnormality Of Connective Tissue

  • Disorder Of Connective Tissue

  • Connective Tissue Disorders

Nervous System Disease
  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder

Dilated Cardiomyopathy
  • Familial Dilated Cardiomyopathy

  • Primary Dilated Cardiomyopathy

  • Idiopathic Dilated Cardiomyopathy

  • Congestive Cardiomyopathy

  • Idiopathic Dilation Cardiomyopathy

  • Primary Familial Dilated Cardiomyopathy

  • Cardiomyopathy, Dilated

  • DCM

  • Cardiomyopathy, Familial Dilated

  • Dilated Cardiomyopathy, Familial

  • Hypokinetic Dilated Cardiomyopathy, Familial

  • Familial Idiopathic Cardiomyopathy

  • Fdc

  • Cardiomyopathy, Familial Idiopathic

  • Idiopathic Cardiomegaly

  • Dilated Congestive Cardiomyopathy

  • Chronic Dilated Cardiomyopathy

  • Ccm - [Congestive Cardiomyopathy]

  • Cocm - [Congestive Cardiomyopathy]

  • Dcm - [Dilated Cardiomyopathy]

  • Dilated-Hypokinetic Cardiomyopathy

  • Congestive Idiopathic Cardiomyopathy

  • Primary Idiopathic Dilated Cardiomyopathy

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus ADIPOQ MGD MGI:106675
Canis familiaris ADIPOQ VGNC VGNC:37656
Bos taurus ADIPOQ VGNC VGNC:25677
Macaca mulatta ADIPOQ VGNC VGNC:69605
Rattus norvegicus ADIPOQ RGD RGD:628748
Felis catus ADIPOQ VGNC VGNC:59641
Others ADIPOQ NCBI