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Diseases
Genes (451)
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ABHD5
Cerebral Creatine Deficiency
TNFRSF1A
Langerhans Cell Histiocytosis
Tumor Necrosis Factor Receptor-Associated Periodic Syndrome
GAMT
Guanidinoacetate Methyltransferase Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
CLCN7
Osteopetrosis, Autosomal Dominant 2
BRAF
Langerhans Cell Histiocytosis
PQBP1
Renpenning's Syndrome
ACP5
Spondyloenchondrodysplasia With Immune Dysregulation
IFIH1
Singleton Merten Syndrome
AR
Langerhans Cell Histiocytosis
Alopecia, Androgenetic, 1
SRD5A2
Alopecia, Androgenetic, 1
RB1
Pinealoblastoma
Trilateral Retinoblastoma
ZFP36
Alopecia, Androgenetic, 1
Familial Isolated Vitamin E Deficiency
MTHFR
Alopecia, Androgenetic, 1
Familial Isolated Vitamin E Deficiency
TNFSF11
Langerhans Cell Histiocytosis
Osteopetrosis, Autosomal Dominant 2
DDX58
Singleton Merten Syndrome
ABCC2
Alopecia, Androgenetic, 1
SUPV3L1
Alopecia, Androgenetic, 1
VDR
Alopecia, Androgenetic, 1
TNFRSF10A
Alopecia, Androgenetic, 1