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Diseases
Genes (466)
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FOXP3
Ipex Syndrome
ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
F12
Factor Xii Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
AP1S1
Mednik Syndrome
FBXO7
Paralysis Agitans, Juvenile, Of Hunt
GALE
Galactose Epimerase Deficiency
TSEN54
Pontocerebellar Hypoplasia, Type 4
MC2R
Familial Glucocorticoid Deficiency
CFH
Membranoproliferative Glomerulonephritis
Factor Xii Deficiency
HBB
Hereditary Persistence Of Fetal Hemoglobin
SLC4A4
Proximal Renal Tubular Acidosis
TSLP
Membranoproliferative Glomerulonephritis
STX3
Microvillus Inclusion Disease
CTNS
Cystinosis
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
HBG1
Hereditary Persistence Of Fetal Hemoglobin