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Diseases
Genes (1187)
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COL2A1
Collagen, Type Ii, Alpha-1
Wagner Vitreoretinopathy
MAT1A
Methionine Adenosyltransferase I/iii Deficiency
Leptospirosis
NLRP3
Behçet's Disease
Familial Cold Autoinflammatory Syndrome 4
Acute Coronary Syndrome
Lichen Planus
COL17A1
Recurrent Corneal Erosion
Pemphigoid
Epithelial Recurrent Erosion Dystrophy
Lichen Planus
SLC20A2
Primary Familial Brain Calcification
Cyclopia
PDGFRB
Primary Familial Brain Calcification
TP63
Behçet's Disease
Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate Syndrome
Lichen Planus
IL10
Leptospirosis
Behçet's Disease
Pemphigoid
Acute Coronary Syndrome
CXCL8
Leptospirosis
Behçet's Disease
Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate Syndrome
Pemphigoid
Acute Coronary Syndrome
TLR4
Leptospirosis
Behçet's Disease
Acute Coronary Syndrome
Lichen Planus
DSP
Epidermolysis Bullosa, Lethal Acantholytic
Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate Syndrome
Pemphigoid
SPINT2
Diarrhea 3, Secretory Sodium, Congenital, With Or Without Other Congenital Anomalies
HLA-B
Behçet's Disease
Acute Coronary Syndrome
NLRC4
Familial Cold Autoinflammatory Syndrome 4
Acute Coronary Syndrome
ERAP1
Behçet's Disease
EGFR
Inflammatory Skin And Bowel Disease, Neonatal, 2
Acute Coronary Syndrome
ERMARD
Periventricular Nodular Heterotopia 3
SLC9A3
Diarrhea 3, Secretory Sodium, Congenital, With Or Without Other Congenital Anomalies
FLNA
Behçet's Disease
Periventricular Nodular Heterotopia 3
VCAN
Coronary Thrombosis
Wagner Vitreoretinopathy