| Diseases |
Alias |
|
| Charcot-Marie-Tooth Disease, Dominant Intermediate E |
|
CMTDIE
|
Charcot-Marie-Tooth Disease Dominant Intermediate E
|
|
Charcot-Marie-Tooth Neuropathy With Focal Segmental Glomerulonephritis
|
Autosomal Dominant Intermediate Charcot-Marie-Tooth Disease Type E
|
|
Charcot-Marie-Tooth Disease-Nephropathy Syndrome
|
Charcot-Marie-Tooth Disease, Dominant, Intermediate Type, E
|
|
Charcot-Marie-Tooth Disease, Dominant Intermediate, Type E
|
|
|
| Focal Segmental Glomerulosclerosis 5 |
|
FSGS5
|
Glomerulosclerosis, Focal Segmental, 5
|
|
Glomerulosclerosis, Segmental, Focal, Type 5
|
|
|
| Focal Segmental Glomerulosclerosis |
|
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome
|
Focal Glomerulosclerosis
|
|
Fsgs
|
Segmental Glomerulosclerosis
|
|
Glomerulosclerosis, Focal Segmental
|
Fgs
|
|
Focal Glomerular Sclerosis
|
Familial Idiopathic Nephrotic Syndrome
|
|
Focal Sclerosis With Hyalinosis
|
Glomerulosclerosis, Focal
|
|
Glomerulosclerosis Focal
|
Glomerulosclerosis, Segmental, Focal
|
|
Focal Segmental Glomerulosclerosis, Not Otherwise Specified
|
|
|
| Genetic Steroid-Resistant Nephrotic Syndrome |
|
Familial Idiopathic Steroid-Resistant Nephrotic Syndrome
|
Genetic Srns
|
|
Hereditary Steroid-Resistant Nephrotic Syndrome
|
Familial Idiopathic Nephrotic Syndrome
|
|
Nephrotic Syndrome, Steroid-Resistant, Autosomal Recessive
|
Srn1
|
|
|
| Nephrotic Syndrome |
|
Finnish Congenital Nephrotic Syndrome
|
Ns - [Nephrotic Syndrome]
|
|
Nephrosis Syndrome
|
Nephrosis Nos
|
|
Glomerular Lesion Nephrosis
|
|
|
| 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
|
|
|
| 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
|
|
|
| Focal Segmental Glomerulosclerosis 6 |
|
FSGS6
|
Glomerulosclerosis, Focal Segmental, 6
|
|
Glomerulosclerosis, Segmental, Focal, Type 6
|
|
|
| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Focal Segmental Glomerulosclerosis 2 |
|
FSGS2
|
Glomerulosclerosis, Focal Segmental, 2
|
|
Glomerulosclerosis, Segmental, Focal, Type 2
|
|
|
| Focal Segmental Glomerulosclerosis 7 |
|
FSGS7
|
Glomerulosclerosis, Focal Segmental, 7
|
|
Glomerulosclerosis, Focal Segmental, Type 7
|
|
|
| Tooth Disease |
|
Tooth Diseases
|
Teeth Disease
|
|
Tooth Disorders
|
|
|
| End Stage Renal Disease |
|
End Stage Renal Failure
|
End-Stage Kidney Disease
|
|
Kidney Failure, Chronic
|
Chronic Kidney Disease Stage 5
|
|
|
| Familial Nephrotic Syndrome |
|
Congenital Nephrotic Syndrome
|
Nephrosis, Congenital
|
|
Finnish Congenital Nephrotic Syndrome
|
|
|
| Focal Segmental Glomerulosclerosis 9 |
|
FSGS9
|
Glomerulosclerosis, Focal Segmental, 9
|
|
Glomerulosclerosis, Focal Segmental, Type 9
|
|
|
| Cerebral Arteritis |
|
Brain Endarteritis
|
Cerebral Or Cerebrospinal Endarteritis
|
|
Brain Arteritis
|
|
|
| Focal Segmental Glomerulosclerosis 8 |
|
FSGS8
|
Glomerulosclerosis, Focal Segmental, 8
|
|
Glomerulosclerosis, Focal Segmental, Type 8
|
|
|
| Oligomeganephronia |
|
Oligomeganephronic Renal Hypoplasia
|
Oligomeganephronic Hypoplasia Of Kidney
|
|
|
| Frasier Syndrome |
|
|
| Pierson Syndrome |
|
Microcoria-Congenital Nephrotic Syndrome
|
Microcoria-Congenital Nephrosis Syndrome
|
|
PIERS
|
Microcoria - Congenital Nephrosis
|
|
Microcoria - Congenital Nephrotic Syndrome
|
PIERSS
|
|
|
| Loeys-Dietz Syndrome 1 |
|
Furlong Syndrome
|
Loeys-Dietz Aortic Aneurysm Syndrome
|
|
LDS1
|
Aat5
|
|
Loeys-Dietz Syndrome Type 1
|
Aortic Aneurysm, Familial Thoracic 5
|
|
Familial Throacic Aortic Aneurysm 5
|
Loeys-Dietz Syndrome
|
|
Aortic Aneurysm Syndrome, Loeys-Dietz Type
|
Familial Thoracic Aortic Aneurysm 5
|
|
Ldas
|
Marfanoid Disorder-Craniosynostosis Syndrome
|
|
Aneurysm, Aortic, Thoracic, Familial, Type 5
|
Loeys-Dietz Syndrome, Type 1
|
|
Loeys-Dietz Syndrome, Type 2a
|
|
|
| Nail-Patella Syndrome |
|
Turner-Kieser Syndrome
|
Onychoosteodysplasia
|
|
Fong Disease
|
NPS
|
|
Hereditary Onycho-Osteodysplasia
|
Nps1
|
|
Hereditary Onychoostedysplasia
|
Iliac Horn Syndrome
|
|
Nail Patella Syndrome
|
Turner-Kiser Syndrome
|
|
Arthro-Onychodysplasia
|
Nps 1
|
|
Osteo-Onychodysplasia
|
Hereditary Osteo-Onychodysplasia
|
|
Osterreicher Syndrome
|
Pelvic Horn Syndrome
|
|
Österreicher-Turner Syndrome
|
Nps - [Nail-Patella Syndrome]
|
|
Hood - [Hereditary Onycho-Osteodysplasia] Syndrome
|
|
|
| Charcot-Marie-Tooth Disease, Axonal, Type 2e |
|
Charcot-Marie-Tooth Disease Type 2
|
CMT2E
|
|
CMT2S
|
CMT2Y
|
|
Charcot-Marie-Tooth Disease Type 2e
|
Charcot-Marie-Tooth Disease Type 2y
|
|
Charcot-Marie-Tooth Disease Axonal Type 2s
|
Charcot-Marie-Tooth Disease, Axonal, Type 2s
|
|
Charcot-Marie-Tooth Disease, Type 2e
|
Hereditary Motor And Sensory Neuropathy Type 2
|
|
Charcot-Marie-Tooth Neuropathy, Type 2s
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2s
|
|
Charcot-Marie-Tooth Disease, Axonal, Type 2y
|
Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2y
|
|
Charcot-Marie-Tooth Neuropathy, Type 2y
|
Charcot-Marie-Tooth Disease, Type 2y
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2e
|
Charcot-Marie-Tooth Neuropathy Type 2e
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Vcp Mutation
|
Cmt2 Due To Vcp Mutation
|
|
Charcot-Marie-Tooth Disease Type 2s
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2
|
|
Autosomal Dominant Axonal Charcot-Marie-Tooth Disease
|
Cmt2
|
|
Charcot-Marie-Tooth Neuropathy, Type 2e
|
Hereditary Motor And Sensory Neuropathy Guadalajara Neuronal Type
|
|
Hereditary Motor And Sensory Neuropathy Okinawa Type
|
Autosomal Dominant Axonal Charcot-Marie-Tooth Type 2y
|
|
Charcot-Marie-Tooth Neuropathy Type 2y
|
Autosomal Recessive Axonal Charcot-Marie-Tooth Type 2s
|
|
Charcot-Marie-Tooth Neuropathy Type 2s
|
Charcot-Marie-Tooth Type 2
|
|
Autosomal Dominant Charcot-Marie-Tooth Disease Type 2y
|
Charcot-Marie-Tooth Disease 2e
|
|
Charcot-Marie-Tooth Disease Axonal Type 2e
|
Charcot-Marie-Tooth Disease Neuronal Type 2e
|
|
Charcot-Marie-Tooth Disease 2s
|
Charcot-Marie-Tooth Neuropathy Axonal Type 2s
|
|
Charcot-Marie-Tooth Disease 2y
|
Charcot-Marie-Tooth Disease, Type 2
|
|
Hereditary Motor And Sensory-Neuropathy Type Ii
|
|
|
| Autosomal Recessive Alport Syndrome |
|
Alport Syndrome, Recessive Type
|
Alport Syndrome, Autosomal Recessive
|
|
Alport Syndrome Autosomal Recessive
|
Alport Syndrome Recessive Type
|
|
Nephropathy And Deafness
|
|
|
| Lipoid Nephrosis |
|
Minimal Change Disease
|
Minimal Change Glomerulonephritis
|
|
Nephrotic Syndrome With Lesion Of Minimal Change Glomerulonephritis
|
Nephrotic Syndrome With Lesion Of Minimal Change Nephrotic Syndrome
|
|
Idiopathic Minimal Change Nephrotic Syndrome
|
Mcns
|
|
Minimal Change Glomerulopathy
|
Minimal Change Nephrotic Syndrome
|
|
Nephrotic Syndrome Minimal Change
|
Nephrosis, Lipoid
|
|
Glomerulonephritis, Minimal Change
|
Nephrotic Syndrome, Minimal Change
|
|
|
| Charcot-Marie-Tooth Disease Intermediate Type |
|
Intermediate Charcot-Marie-Tooth Disease
|
Charcot-Marie-Tooth Disease Dominant Intermediate
|
|
Charcot-Marie-Tooth Disease Recessive Intermediate
|
Intermediate Cmt
|
|
Intermediate Hereditary Motor And Sensory Neuropathy
|
Charcot-Marie-Tooth Disease, Intermediate Type
|
|
Charcot-Marie-Tooth, Intermediate
|
|
|
| Alport Syndrome |
|
Hereditary Nephritis
|
Alport Syndrome, X-Linked
|
|
Hemorrhagic Hereditary Nephritis
|
Congenital Hereditary Hematuria
|
|
Hemorrhagic Familial Nephritis
|
Familial Nephritis
|
|
Thin Basement Membrane Disease
|
Thin Basement Membrane Nephropathy
|
|
Hematuria-Nephropathy-Deafness Syndrome
|
Hematuric Hereditary Nephritis
|
|
Hereditary Familial Congenital Hemorrhagic Nephritis
|
Hereditary Hematuria Syndrome
|
|
Hereditary Interstitial Pyelonephritis
|
Alport Deafness-Nephropathy
|
|
Alport Hearing Loss-Nephropathy
|
Alports Syndrome
|
|
Nephritis, Hereditary
|
|
|
| Denys-Drash Syndrome |
|
Drash Syndrome
|
DDS
|
|
Nephropathy, Wilms Tumor, And Genital Anomalies
|
Wilms Tumor And Pseudohermaphroditism
|
|
Wilms Tumor And Pseudo- Or True Hermaphroditism
|
Nephropathy Associated With Male Pseudohermaphroditism And Wilms' Tumor
|
|
Pseudohermaphroditism, Nephron Disorder And Wilms' Tumor
|
Wilms Tumor-Dsd Syndrome
|
|
Wilms Tumor-Disorder Of Sex Development Syndrome
|
|
|
| Galloway-Mowat Syndrome |
|
Galloway Mowat Syndrome
|
Galloway Syndrome
|
|
Hiatal Hernia-Microcephaly-Nephrosis, Galloway Type
|
Microcephaly Nephrosis Syndrome
|
|
Microcephaly, Hiatal Hernia, And Nephrotic Syndrome
|
Nephrosis Neuronal Dysmigration Syndrome
|
|
Microcephaly-Hiatus Hernia-Nephrotic Syndrome
|
Nephrosis-Neuronal Dysmigration Syndrome
|
|
|
| 3-Methylglutaconic Aciduria, Type Iii |
|
Optic Atrophy
|
3-Methylglutaconic Aciduria Type 3
|
|
Costeff Syndrome
|
Mga3
|
|
Costeff Optic Atrophy Syndrome
|
Optic Atrophy Plus Syndrome
|
|
Infantile Optic Atrophy With Chorea And Spastic Paraplegia
|
3-Methylglutaconic Aciduria Type Iii
|
|
Autosomal Recessive Optic Atrophy Plus Syndrome
|
Autosomal Recessive Optic Atrophy Type 3
|
|
Opa3 Defect
|
MGCA3
|
|
Mga, Type Iii
|
Iraqi Jewish Optic Atrophy Plus
|
|
Mga Type Iii
|
Optic Atrophy, Infantile, With Chorea And Spastic Paraplegia
|
|
Iraqi-Jewish 'Optic Atrophy Plus'
|
Optic Atrophy 3, Autosomal Recessive
|
|
Opa3, Autosomal Recessive
|
Opa3-Related 3-Methylglutaconic Aciduria
|
|
Iraqi-Jewish Optic Atrophy Plus
|
Atrophy Of Optic Disc
|
|
3-Alpha Methylglutaconic Aciduria Type Iii
|
Optic Atrophy 3
|
|
Optic Atrophy Infantile With Chorea And Spastic Paraplegia
|
Autosomal Recessive Opa3
|
|
Autosomal Recessive Optic Atrophy 3
|
3-Methylglutaconic Aciduria 3
|
|
3-Alpha-Methylglutaconic Aciduria Type 3
|
Optic Atrophy 3 Autosomal Recessive
|
|
Atrophy, Optic
|
Atrophy, Optic, Plus Syndrome
|
|
Optic Nerve Atrophy
|
Primary Optic Atrophy
|
|
Oa - [Optic Atrophy]
|
Second Cranial Nerve Atrophy
|
|
Second Cranium Nerve Atrophy
|
|
|
| Hemolytic Uremic Syndrome, Atypical 1 |
|
Atypical Hemolytic-Uremic Syndrome
|
Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1
|
|
Atypical Hemolytic Uremic Syndrome
|
Hemolytic Uremic Syndrome, Atypical, Susceptibility To
|
|
Ahus
|
AHUS1
|
|
Hemolytic-Uremic Syndrome
|
Ahus 1
|
|
Ahus, Susceptibility To, 1
|
Hemolytic Uremic Syndrome, Atypical
|
|
Non-Shiga-Like Toxin-Associated Hus
|
Non-Stx-Hus
|
|
Nonenteropathic Hus
|
Atypical Hus
|
|
Shiga Toxin-Associated Hemolytic Uremic Syndrome
|
D+ Hus
|
|
Ehec-Hus
|
Hemolytic Uremic Syndrome Associated With Shiga Toxin-Producing Escherichia Coli
|
|
Hemolytic Uremic Syndrome With Diarrhea
|
Stec-Hus
|
|
Shiga-Like Toxin-Associated Hus
|
Stx-Hus
|
|
Typical Hus
|
Typical Hemolytic Uremic Syndrome
|
|
Atypical Hemolytic Uremic Syndrome With Anti-Factor H Antibodies
|
Atypical Hus With Anti-Factor H Antibodies
|
|
Ahus With Anti-Factor H Antibodies
|
Ahus With Neutralizing Autoantibodies Against Factor H
|
|
Hemolytic Uremic Syndrome Atypical 1
|
Atypical Hemolytic Uremic Syndrome With H Factor Anomaly
|
|
D Hus
|
Hemolytic-Uremic Syndrome Without Diarrhea
|
|
Hemolytic-Uremic Syndrome, Atypical, Type 1
|
Hemolytic Uremic Syndrome, Typical
|
|
|
| Neuromuscular Disease |
|
Neuromuscular Diseases
|
Neuromuscular Disorders
|
|
Neuromuscular Disorder
|
|
|
