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Diseases
Genes (688)
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MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
FAM20A
Enamel-Renal Syndrome
MC2R
Familial Glucocorticoid Deficiency
HLA-DRB1
Sarcoidosis, Susceptibility To, 1
BTNL2
Sarcoidosis, Susceptibility To, 1
IFIH1
Singleton Merten Syndrome
STX3
Microvillus Inclusion Disease
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
ANXA11
Sarcoidosis, Susceptibility To, 1
MRAP
Familial Glucocorticoid Deficiency
RB1
Pinealoblastoma
Trilateral Retinoblastoma
IL18
Sarcoidosis, Susceptibility To, 1
HLA-DPB1
Sarcoidosis, Susceptibility To, 1
TGFB1
Sarcoidosis, Susceptibility To, 1
Melorheostosis
LEMD3
Melorheostosis
SLC11A1
Sarcoidosis, Susceptibility To, 1