| Diseases |
Alias |
|
| Congenital Disorder Of Glycosylation, Type Iiq |
|
CDG2Q
|
Cdg Iiq
|
|
Cdgiiq
|
Congenital Disorder Of Glycosylation Type Iiq
|
|
Cog2-Cdg
|
Cog2-Related Congenital Disorder Of Glycosylation
|
|
Cdgiidq
|
Congenital Disorder Of Glycosylation 2q
|
|
Cdg-Iiq
|
|
|
| Congenital Disorder Of Glycosylation, Type Iig |
|
CDG2G
|
Congenital Disorder Of Glycosylation Type Iig
|
|
Cdg Iig
|
Cdgiig
|
|
Cdgii/Cog1 Cerebrocostomandibular-Like Syndrome
|
Carbohydrate Deficient Glycoprotein Syndrome Type Iig
|
|
Cdg-Iig
|
Congenital Disorder Of Glycosylation, Type 2g
|
|
Cog1-Cdg
|
Cdg Syndrome Type Iig
|
|
Congenital Disorder Of Glycosylation Type 2g
|
Congenital Disorder Of Glycosylation 2g
|
|
Cdg-Ii Caused By Cog1 Deficiency
|
Glycosylation, Congenital Disorder Of, Type Iig
|
|
|
| Congenital Disorder Of Glycosylation, Type Iil |
|
CDG2L
|
Congenital Disorder Of Glycosylation Type Iil
|
|
Cdg Iil
|
Cog6-Cgd
|
|
Cdgiil
|
Cdg Syndrome Type Iil
|
|
Congenital Disorder Of Glycosylation Type 2l
|
Cdg-Iil
|
|
Cdgiidl
|
Congenital Disorder Of Glycosylation 2l
|
|
Glycosylation, Congenital Disorder Of, Type Iil
|
|
|
| Familial Hypercholesterolemia |
|
Hyperlipoproteinemia Type Iia
|
Familial Hyperbetalipoproteinaemia
|
|
Familial Hypercholesteremia
|
Fredrickson Type Iia Hyperlipoproteinemia
|
|
Fredrickson Type Iia Lipidaemia
|
Hyperbetalipoproteinemia
|
|
Type Ii Hyperlipidemia
|
Familial Hypercholesterolæmia
|
|
Familial Hypercholesterolaemia
|
Fh
|
|
Hypercholesterolemia Familial
|
Hyperlipoproteinemia Type Ii
|
|
Hypercholesterolemia, Familial
|
|
|
| Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 |
|
Distal Spinal Muscular Atrophy Type 3
|
DSMA3
|
|
Spinal Muscular Atrophy, Chronic Distal, Autosomal Recessive
|
Autosomal Recessive Distal Spinal Muscular Atrophy Type 3
|
|
Dhmn3 And Dhmn4
|
Distal Hereditary Motor Neuropathy Type 3 And Type 4
|
|
Neuronopathy, Distal Hereditary Motor, Type Iv
|
Hmn4
|
|
Dhmn4
|
Neuropathy, Distal Hereditary Motor, Type Iv
|
|
Hmn Iv
|
Neuronopathy, Distal Hereditary Motor, Type Iii
|
|
Hmn3
|
Dhmn3
|
|
Hmn Iii
|
|
|
| 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
|
|
|
| Hypercholesterolemia, Familial, 1 |
|
Hypercholesterolemia
|
FHCL1
|
|
Fhc
|
Fh
|
|
Hyperlipoproteinemia, Type Ii
|
Hyperlipoproteinemia, Type Iia
|
|
Hyper-Low-Density-Lipoproteinemia
|
Hypercholesterolemic Xanthomatosis, Familial
|
|
Ldl Receptor Disorder
|
Hypercholesterolemia, Susceptibility To
|
|
Hypercholesterolemia, Familial, Modifier Of
|
Hypercholesterolemia, Familial, Due To Ldlr Defect, Modifier Of
|
|
Ldl Cholesterol Level Qtl2
|
Hyperlipoproteinemia Type Ii
|
|
Hypercholesterolemia, Familial, Type 1
|
High Cholesterol
|
|
Increased Cholesterol
|
Low-Density-Lipoid-Type Hyperlipoproteinemia
|
|
Pure Hypercholesterolaemia
|
Ldl - [Low Density Lipoprotein} Hyperlipoproteinemia
|
|
Group A Hyperlipidaemia
|
Pure Hypercholesterinaemia
|
|
Cholesterolaemia
|
Essential Cholesterolaemia
|
|
Essential Hypercholesterolaemia
|
Group A Hyperlipemia
|
|
Increased Low Density Lipoprotein
|
Low-Density-Lipoprotein-Type
|
|
Low-Density-Lipoprotein-Type Hyperlipoproteinemia
|
|
|
| Immunodeficiency 47 |
|
Congenital Disorder Of Glycosylation Type Ii
|
CDG2E
|
|
Congenital Disorder Of Glycosylation Type Iie
|
IMD47
|
|
Cdg2s
|
Cdg Iis
|
|
Cdgiis
|
Immunodeficiency And Hepatopathy With Or Without Neurologic Features
|
|
Congenital Disorder Of Glycosylation, Type Ii
|
CDG1I
|
|
Congenital Disorder Of Glycosylation, Type Iie
|
Cdg Iie
|
|
Congenital Disorder Of Glycosylation Type 2e
|
Congenital Disorder Of Glycosylation, Type Iis
|
|
Cdg Ii
|
Cdgii
|
|
Cdgiie
|
Carbohydrate Deficient Glycoprotein Syndrome Type Iie
|
|
Cdg Syndrome Type Iie
|
Congenital Disorder Of Glycosylation Ii
|
|
Congenital Disorder Of Glycosylation 1i
|
Cdg-Iie
|
|
Alg2-Cdg
|
Cdg-Ii
|
|
Glycosylation, Congenital Disorder Of, Type Ii
|
Cdgiide
|
|
Congenital Disorder Of Glycosylation Type Iis
|
Cog7-Cdg
|
|
Cdg Syndrome Type Ii
|
Carbohydrate Deficient Glycoprotein Syndrome Type Ii
|
|
Congenital Disorder Of Glycosylation Type 1i
|
Mannosyltransferase 2 Deficiency
|
|
Congenital Disorder Of Glycosylation 2e
|
Congenital Disorder Of Glycosylation 2s
|
|
Congenital Disorders Of Glycosylation Type Ii
|
Glycosylation, Congenital Disorder Of, Type Iie
|
|
Immunodeficiency, Type 47
|
Congenital Disorder Of Glycosylation Type 2a
|
|
|
| Congenital Disorder Of Glycosylation, Type Iih |
|
CDG2H
|
Congenital Disorder Of Glycosylation Type Iih
|
|
Cdg Iih
|
Cdgiih
|
|
Carbohydrate Deficient Glycoprotein Syndrome Type Iih
|
Congenital Disorder Of Glycosylation Type 2h
|
|
Cog8-Cdg
|
Cdg-Iih
|
|
Cdgiidh
|
Cdg Syndrome Type Iih
|
|
Congenital Disorder Of Glycosylation 2h
|
Glycosylation, Congenital Disorder Of, Type Iih
|
|
|
| Congenital Disorder Of Glycosylation, Type Iij |
|
CDG2J
|
Congenital Disorder Of Glycosylation Type Iij
|
|
Cdg Iij
|
Cdgiij
|
|
Carbohydrate Deficient Glycoprotein Syndrome Type Iij
|
Cdg Syndrome Type Iij
|
|
Congenital Disorder Of Glycosylation Type 2j
|
Cog4-Cdg
|
|
Cdg-Iij
|
Cdgiidj
|
|
Congenital Disorder Of Glycosylation 2j
|
Glycosylation, Congenital Disorder Of, Type Iij
|
|
|
| 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
|
|
|
| Galactosemia Iii |
|
Galactose Epimerase Deficiency
|
Gale Deficiency
|
|
Udp-Galactose-4-Epimerase Deficiency
|
Epimerase Deficiency Galactosemia
|
|
Galactosemia Type 3
|
Gale-D
|
|
Uridine Diphosphate Galactose-4-Epimerase Deficiency
|
GALAC3
|
|
Galactosemia 3
|
Generalized Uridine Diphosphate Galactose-4-Epimerase Deficiency
|
|
Erythrocyte Uridine Diphosphate Galactose-4-Epimerase Deficiency
|
Galactosemia Type Iii
|
|
Udp-Galactose-4'-Epimerase Deficiency
|
Generalized Galactose Epimerase Deficiency
|
|
Generalized Gale Deficiency
|
Generalized Gale-D
|
|
Generalized Udp-Galactose-4-Epimerase Deficiency
|
Generalized Epimerase Deficiency Galactosemia
|
|
Erythrocyte Galactose Epimerase Deficiency
|
Erythrocyte Gale Deficiency
|
|
Erythrocyte Gale-D
|
Erythrocyte Udp-Galactose-4-Epimerase Deficiency
|
|
Erythrocyte Epimerase Deficiency Galactosemia
|
Galactosemias
|
|
Classical Galactosemia
|
Udpglucose 4-Epimerase Deficiency Disease
|
|
|
| Hyperlipoproteinemia, Type Iii |
|
Hyperlipoproteinemia Type Iii
|
Broad-Betalipoproteinemia
|
|
Floating-Betalipoproteinemia
|
Familial Type 3 Hyperlipoproteinemia
|
|
Broad Beta Disease
|
Familial Hyperbeta- And Prebetalipoproteinemia
|
|
Familial Hypercholesterolemia With Hyperlipemia
|
Hyperlipemia With Familial Hypercholesterolemic Xanthomatosis
|
|
Coronary Artery Disease, Severe, Susceptibility To
|
Coronary Artery Disease, Severe
|
|
Hyperlipidemia Type 3
|
Familial Dysbetalipoproteinemia
|
|
Hyperlipoproteinemia Type 3
|
Coronary Artery Disease
|
|
Apolipoprotein E, Deficiency Or Defect Of
|
Dysbetalipoproteinemia Due To Defect In Apolipoprotein E-D
|
|
Carbohydrate Induced Hyperlipemia
|
Familial Hypercholesterolaemia With Hyperlipaemia
|
|
Remnant Hyperlipidemia
|
Remnant Removal Disease
|
|
Dysbetalipoproteinemia
|
Broad-Beta Disease
|
|
Familial Dyslipidemia Type 3
|
Hlp Type 3
|
|
Remnant Hyperlipoproteinemia
|
Familial Hyperlipoproteinemia Type Iii
|
|
CAD
|
Hyperlipoproteinemia 3
|
|
HLPP3
|
Deficiency Or Defect Of Apolipoprotein E
|
|
Dysbetalipoproteinemia Due To Defect In Apolipoprotein E
|
Coronary Arteriosclerosis
|
|
Coronary Heart Disease
|
|
|
| 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
|
|
|
| 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
|
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| Congenital Hypothyroidism |
|
Cretinism
|
Neonatal Hypothyroidism
|
|
Ch
|
Cht
|
|
Congenital Myxedema
|
Myxedema, Congenital
|
|
Endemic Cretinism
|
Congenital Iodine-Deficiency Syndrome
|
|
Fetal Iodine Deficiency Syndrome
|
Congenital Iodine-Deficiency Hypothyroidism Nos
|
|
|
| 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
|
|
|
| Congenital Disorder Of Glycosylation, Type In |
|
Congenital Disorder Of Glycosylation
|
CDG1N
|
|
Congenital Disorders Of Glycosylation
|
Cdg In
|
|
Cdgin
|
Congenital Disorder Of Glycosylation 1n
|
|
Carbohydrate-Deficient Glycoprotein Syndrome
|
Cdg
|
|
Rft1-Cdg
|
Cdg-In
|
|
Congenital Disorder Of Glycosylation Type In
|
Carbohydrate Deficient Glycoprotein Syndrome
|
|
Cdg Syndrome
|
Congenital Disorder Of Glycosylation In
|
|
Carbohydrate-Deficient Glycoprotein Syndromes
|
Cdg Syndrome Type In
|
|
Carbohydrate Deficient Glycoprotein Syndrome Type In
|
Congenital Disorder Of Glycosylation Type 1n
|
|
Man5glcnac2-Pp-Dol Flippase Deficiency
|
Glycosylation, Congenital Disorder Of
|
|
Glycosylation, Congenital Disorder Of, Type In
|
|
|
| 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
|
|
|
| Diabetes Mellitus |
|
|
| 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
|
|
|
