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Diseases
Genes (666)
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ABHD5
Cerebral Creatine Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
CTNS
Cystinosis
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
PRKAR1A
Alopecia, Androgenetic, 1
Enamel-Renal Syndrome
IFNG
Hepatitis E
Cerebral Creatine Deficiency
Type Iii Hypersensitivity
Cryptococcosis
Vascular Tumor
Cystinosis
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CNBP
Cryptococcosis
Myotonic Dystrophy
ZFP36
Alopecia, Androgenetic, 1
Familial Isolated Vitamin E Deficiency
Vascular Tumor
DDX58
Hepatitis E
Singleton Merten Syndrome