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Diseases
Genes (1527)
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ABHD5
Cerebral Creatine Deficiency
ABCD1
Adrenoleukodystrophy
GAMT
Guanidinoacetate Methyltransferase Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
TNF
Alopecia, Androgenetic, 1
Persistent Truncus Arteriosus
Adrenoleukodystrophy
Hyperinsulinism
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Uterine Fibroids
Morphea
KCNC3
Spinocerebellar Ataxia Type-13
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
LEP
Alopecia, Androgenetic, 1
Hyperinsulinism
Uterine Fibroids
IFIH1
Singleton Merten Syndrome
NKX2-6
Persistent Truncus Arteriosus
TP63
Bladder Exstrophy
Uterine Fibroids
HMOX1
Adrenoleukodystrophy
Hyperinsulinism
CCL2
Adrenoleukodystrophy
Hyperinsulinism
Uterine Fibroids
PLXND1
Persistent Truncus Arteriosus
TSC2
Uterine Fibroids
AR
Alopecia, Androgenetic, 1
Hyperinsulinism
Uterine Fibroids
ASS1
Citrullinemia Type I
INSR
Hyperinsulinism
Uterine Fibroids
ESR1
Cerebral Creatine Deficiency
Hyperinsulinism
Uterine Fibroids