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Diseases
Genes (995)
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KRT17
Pachyonychia Congenita
KRT16
Skin Condition
Pachyonychia Congenita
ACE
Severe Acute Respiratory Syndrome
PSEN1
Cognitive Deficit
MAPT
Cognitive Deficit
APP
Cognitive Deficit
APOE
Cognitive Deficit
COMT
Cognitive Deficit
FMR1
Cognitive Deficit
MED12
Fibroadenoma
GFI1B
Platelet Storage Pool Deficiency
KRT6A
Pachyonychia Congenita
GSK3B
Cognitive Deficit
BCHE
Cognitive Deficit
PTGS2
Cognitive Deficit
DRD2
Cognitive Deficit
RARA
Fibroadenoma
PMP22
Locked-In Syndrome
TBCD
Locked-In Syndrome
KRT10
Skin Condition
Pachyonychia Congenita