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Diseases
Genes (394)
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ABHD5
Cerebral Creatine Deficiency
MYO5B
Microvillus Inclusion Disease
GAMT
Guanidinoacetate Methyltransferase Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
HNF1A
Hepatocellular Adenoma
STX3
Microvillus Inclusion Disease
A2M
Hepatocellular Adenoma
SRD5A2
Alopecia, Androgenetic, 1
AR
Alopecia, Androgenetic, 1
PRKAR1A
Alopecia, Androgenetic, 1
Hepatocellular Adenoma
CTNNB1
Alopecia, Androgenetic, 1
Hepatocellular Adenoma
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
VDR
Alopecia, Androgenetic, 1
Lumbar Disc Disease
CILP
Lumbar Disc Disease
ABCC2
Alopecia, Androgenetic, 1
Hepatocellular Adenoma
MTHFR
Alopecia, Androgenetic, 1
Hepatocellular Adenoma
TNFRSF10A
Alopecia, Androgenetic, 1
Lumbar Disc Disease
COL9A3
Lumbar Disc Disease