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Diseases
Genes (1094)
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OPN1LW
Colorblindness, Partial, Protan Series
Blue Cone Monochromacy
PAX6
Aniridia 2
MSH2
Colorectal Cancer, Hereditary Nonpolyposis, Type 8
MLH1
Colorectal Cancer, Hereditary Nonpolyposis, Type 8
TP53
Colorectal Cancer, Hereditary Nonpolyposis, Type 8
Leukemia, Chronic Lymphocytic, Susceptibility To, 4
Basal Cell Carcinoma, Susceptibility To, 7
PMS2
Colorectal Cancer, Hereditary Nonpolyposis, Type 8
MSH6
Colorectal Cancer, Hereditary Nonpolyposis, Type 8
CYP11B1
Hyperaldosteronism, Familial, Type I
OPN1MW
Blue Cone Monochromacy
Pain Asymbolia
PNPO
Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency
NT5C3A
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due To
MLH3
Colorectal Cancer, Hereditary Nonpolyposis, Type 8
EPCAM
Colorectal Cancer, Hereditary Nonpolyposis, Type 8
ATXN8
Spinocerebellar Ataxia 8
ATM
Colorectal Cancer, Hereditary Nonpolyposis, Type 8
Leukemia, Chronic Lymphocytic, Susceptibility To, 4
SMARCD1
Foot Deformity
Hand Deformity
PIGB
Foot Deformity
Hand Deformity
TRIM44
Aniridia 2
KRAS
Cubitus Valgus
Genu Recurvatum
Colorectal Cancer, Hereditary Nonpolyposis, Type 8
TGFBR2
Colorectal Cancer, Hereditary Nonpolyposis, Type 8