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Diseases
Genes (1290)
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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
COL17A1
Pemphigoid
Recurrent Corneal Erosion
Epithelial Recurrent Erosion Dystrophy
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
PDGFRB
Bone Cyst
Primary Familial Brain Calcification
IL10
Leptospirosis
Behçet's Disease
Pemphigoid
Acute Coronary Syndrome
DSP
Pemphigoid
Epidermolysis Bullosa, Lethal Acantholytic
Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate Syndrome
Naxos Disease
TLR4
Callosity
Leptospirosis
Behçet's Disease
Acute Coronary Syndrome
Lichen Planus
CXCL8
Leptospirosis
Behçet's Disease
Pemphigoid
Ankyloblepharon-Ectodermal Defects-Cleft Lip/palate Syndrome
Acute Coronary Syndrome
SPINT2
Diarrhea 3, Secretory Sodium, Congenital, With Or Without Other Congenital Anomalies
SLC20A2
Primary Familial Brain Calcification
NLRC4
Familial Cold Autoinflammatory Syndrome 4
Acute Coronary Syndrome
HLA-B
Behçet's Disease
Acute Coronary Syndrome
FLNA
Behçet's Disease
Periventricular Nodular Heterotopia 3
Aneurysm Of Sinus Of Valsalva
ERMARD
Periventricular Nodular Heterotopia 3
SLC9A3
Diarrhea 3, Secretory Sodium, Congenital, With Or Without Other Congenital Anomalies
EGFR
Inflammatory Skin And Bowel Disease, Neonatal, 2
Acute Coronary Syndrome
ERAP1
Behçet's Disease