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Diseases
Genes (483)
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SH3TC2
Charcot-Marie-Tooth Neuropathy Type 4c
ADAR
Dyschromatosis Symmetrica Hereditaria
KRT17
Pachyonychia Congenita
KRT16
Pachyonychia Congenita
GRIN2A
Rolandic Epilepsy
ACE
Severe Acute Respiratory Syndrome
Dyschromatosis Symmetrica Hereditaria
KRT6A
Pachyonychia Congenita
MBTPS2
Keratosis Follicularis Spinulosa Decalvans
SAT1
Keratosis Follicularis Spinulosa Decalvans
KRT6B
Pachyonychia Congenita
LRP1
Keratosis Follicularis Spinulosa Decalvans
Lipoma
PLAT
Bloodstream Infections
Locked-In Syndrome
CISH
Bloodstream Infections
SRPX2
Rolandic Epilepsy
CXCL1
Severe Acute Respiratory Syndrome
Bloodstream Infections
TIRAP
Bloodstream Infections
GABRG2
Rolandic Epilepsy
PMP22
Charcot-Marie-Tooth Neuropathy Type 4c
Locked-In Syndrome
CXCL6
Severe Acute Respiratory Syndrome
HBA1
Hemoglobin H Disease