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Diseases
Genes (842)
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ABHD5
Cerebral Creatine Deficiency
COL2A1
Spondyloepiphyseal Dysplasia Congenita
Chondrodystrophy
GAMT
Guanidinoacetate Methyltransferase Deficiency
MYO5B
Microvillus Inclusion Disease
SLC4A11
Chandler's Syndrome
Corneal Dystrophy And Perceptive Deafness
FMR1
Fragile X-Associated Tremor/ataxia Syndrome
LIM2
Cataract 19, Multiple Types
SLC17A5
Salla Disease
NGLY1
Ngly1 Deficiency
MC2R
Familial Glucocorticoid Deficiency
TNF
Alopecia, Androgenetic, 1
Hypoglycemia
Asthma Attack
Pulmonary Edema
Salla Disease
NOS3
High-Altitude Pulmonary Edema
Pulmonary Edema
CRH
Alopecia, Androgenetic, 1
Hypoglycemia
STX3
Microvillus Inclusion Disease
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
PTEN
Anisometropia
Hypoglycemia
PGM1
Hypoglycemia
Ngly1 Deficiency
ABCC8
Hypoglycemia
IGF2
Hypoglycemia