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Diseases
Genes (1066)
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ABHD5
Cerebral Creatine Deficiency
ABCD1
Adrenoleukodystrophy
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
KCNC3
Spinocerebellar Ataxia Type-13
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
GALE
Galactose Epimerase Deficiency
MC2R
Familial Glucocorticoid Deficiency
TP63
Uterine Fibroids
Bladder Exstrophy
CFH
Membranoproliferative Glomerulonephritis
TSC2
Uterine Fibroids
STX3
Microvillus Inclusion Disease
HMGA2
Uterine Fibroids
AR
Alopecia, Androgenetic, 1
Uterine Fibroids
TSLP
Membranoproliferative Glomerulonephritis
CTNS
Cystinosis
SRD5A2
Alopecia, Androgenetic, 1
ISL1
Bladder Exstrophy
ESR1
Cerebral Creatine Deficiency
Uterine Fibroids
MRAP
Familial Glucocorticoid Deficiency