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Diseases
Genes (575)
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ABHD5
Cerebral Creatine Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
GAMT
Guanidinoacetate Methyltransferase Deficiency
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
AGGF1
Klippel-Trenaunay-Weber Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
PRKAR1A
Alopecia, Androgenetic, 1
Enamel-Renal Syndrome
RB1
Pinealoblastoma
Trilateral Retinoblastoma
CNBP
Myotonic Dystrophy
Cryptococcosis
ZFP36
Alopecia, Androgenetic, 1
Familial Isolated Vitamin E Deficiency
Vascular Tumor
IFNG
Cerebral Creatine Deficiency
Type Iii Hypersensitivity
Vascular Tumor
Cryptococcosis
SOST
Klippel-Trenaunay-Weber Syndrome
Craniodiaphyseal Dysplasia
MTHFR
Alopecia, Androgenetic, 1
Familial Isolated Vitamin E Deficiency
BRD4
Alopecia, Androgenetic, 1
Cryptococcosis
DDX58
Singleton Merten Syndrome