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Diseases
Genes (433)
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ABHD5
Cerebral Creatine Deficiency
TNFRSF1A
Langerhans Cell Histiocytosis
Tumor Necrosis Factor Receptor-Associated Periodic Syndrome
GAMT
Guanidinoacetate Methyltransferase Deficiency
CLCN7
Osteopetrosis, Autosomal Dominant 2
BRAF
Langerhans Cell Histiocytosis
COL2A1
Collagen, Type Ii, Alpha-1
ACP5
Spondyloenchondrodysplasia With Immune Dysregulation
IFIH1
Singleton Merten Syndrome
PAH
Phenylketonuria
AR
Langerhans Cell Histiocytosis
Alopecia, Androgenetic, 1
SRD5A2
Alopecia, Androgenetic, 1
RB1
Pinealoblastoma
Trilateral Retinoblastoma
IFNG
Cerebral Creatine Deficiency
Langerhans Cell Histiocytosis
Osteopetrosis, Autosomal Dominant 2
Pleural Disease
TGFB1
Alopecia, Androgenetic, 1
Pleural Disease
IL6
Tumor Necrosis Factor Receptor-Associated Periodic Syndrome
Pleural Disease
TNFSF11
Langerhans Cell Histiocytosis
Osteopetrosis, Autosomal Dominant 2
DDX58
Singleton Merten Syndrome
CCL2
Tumor Necrosis Factor Receptor-Associated Periodic Syndrome
Pleural Disease
ABCC2
Alopecia, Androgenetic, 1
SUPV3L1
Alopecia, Androgenetic, 1