Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Slow acetylator due to N-acetyltransferase enzyme variant
20 0 4 0.13 0 0
CUI: C3203670
Disease: NAT2 polymorphism
NAT2 polymorphism
3 0 2 0.12 0 0
CUI: C0028797
Disease: Occupational Diseases
Occupational Diseases
22 0 4 0.12 0 0
CUI: C0860168
Disease: Distal colitis
Distal colitis
6 0 2 0.11 0 0
CUI: C4728019
Disease: Acute on chronic hepatitis B
Acute on chronic hepatitis B
21 0 3 9.1E-02 0 0
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma
24 0 3 8.3E-02 0 0
ADRENOCORTICAL CARCINOMA, HEREDITARY
13 0 2 7.7E-02 0 0
CUI: C0004403
Disease: Autosome Abnormalities
Autosome Abnormalities
16 0 2 6.9E-02 0 0
CUI: C0007121
Disease: Bronchogenic Carcinoma
Bronchogenic Carcinoma
47 0 4 6.9E-02 0 0
CUI: C0008625
Disease: Chromosome Aberrations
Chromosome Aberrations
16 0 2 6.9E-02 0 0
CUI: C0023441
Disease: Leukemia, Experimental
Leukemia, Experimental
1 0 1 6.7E-02 0 0
CUI: C0231450
Disease: Abnormal extension
Abnormal extension
1 0 1 6.7E-02 0 0
CUI: C0277337
Disease: Infection by Polymorphus
Infection by Polymorphus
1 0 1 6.7E-02 0 0
CUI: C0349539
Disease: Malignant melanoma of rectum
Malignant melanoma of rectum
1 0 1 6.7E-02 0 0
CUI: C0544862
Disease: Neurocutaneous melanosis
Neurocutaneous melanosis
1 0 1 6.7E-02 0 0
childhood acute myeloid leukemia/other myeloid malignancies
1 0 1 6.7E-02 0 0
CUI: C1334691
Disease: Melanomatosis
Melanomatosis
1 0 1 6.7E-02 0 0
Fast acetylator due to N-acetyltransferase enzyme variant
17 0 2 6.7E-02 0 0
Spondylocostal Dysostosis with Anal Atresia and Urogenital Anomalies
1 0 1 6.7E-02 0 0
CUI: C1969649
Disease: KALA-AZAR, SUSCEPTIBILITY TO, 2
KALA-AZAR, SUSCEPTIBILITY TO, 2
1 0 1 6.7E-02 0 0
CUI: C2674383
Disease: Cerebellar stroke
Cerebellar stroke
1 0 1 6.7E-02 0 0
LOW DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6
1 0 1 6.7E-02 0 0
CUI: C3805812
Disease: NEUROCUTANEOUS MELANOSIS, SOMATIC
NEUROCUTANEOUS MELANOSIS, SOMATIC
1 0 1 6.7E-02 0 0
Numerous congenital melanocytic nevi
1 0 1 6.7E-02 0 0
CUI: C3888516
Disease: CYP1A2 polymorphism
CYP1A2 polymorphism
1 0 1 6.7E-02 0 0