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Diseases
Genes (1112)
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MAT1A
Methionine Adenosyltransferase I/iii Deficiency
Leptospirosis
JUP
Epidermolysis Bullosa, Lethal Acantholytic
Acute Coronary Syndrome
Naxos Disease
NLRP3
Behçet's Disease
Familial Cold Autoinflammatory Syndrome 4
Acute Coronary Syndrome
Lichen Planus
MMP2
Methionine Adenosyltransferase I/iii Deficiency
Behçet's Disease
Acute Coronary Syndrome
Lichen Planus
Multicentric Osteolysis, Nodulosis, And Arthropathy
TP63
Behçet's Disease
Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate Syndrome
Lichen Planus
IL10
Leptospirosis
Behçet's Disease
Acute Coronary Syndrome
DSP
Epidermolysis Bullosa, Lethal Acantholytic
Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate Syndrome
Naxos Disease
COL17A1
Recurrent Corneal Erosion
Epithelial Recurrent Erosion Dystrophy
Lichen Planus
TLR4
Leptospirosis
Behçet's Disease
Acute Coronary Syndrome
Lichen Planus
SPINT2
Diarrhea 3, Secretory Sodium, Congenital, With Or Without Other Congenital Anomalies
SLC20A2
Primary Familial Brain Calcification
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
FLNA
Behçet's Disease
Periventricular Nodular Heterotopia 3
Aneurysm Of Sinus Of Valsalva
ERMARD
Periventricular Nodular Heterotopia 3
PDGFRB
Primary Familial Brain Calcification
SLC9A3
Diarrhea 3, Secretory Sodium, Congenital, With Or Without Other Congenital Anomalies
VCAN
Coronary Thrombosis
Wagner Vitreoretinopathy