Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0028425
Disease: Crusted scabies
Crusted scabies 		1 0 1 5.3E-02 0 0
CUI: C0341248
Disease: Chronic duodenitis
Chronic duodenitis 		1 0 1 5.3E-02 0 0
CUI: C0495452
Disease: Noninfective neonatal diarrhea
Noninfective neonatal diarrhea 		1 0 1 5.3E-02 0 0
CUI: C0496784
Disease: Malignant neoplasm of endocrine pancreas
Malignant neoplasm of endocrine pancreas 		1 0 1 5.3E-02 0 0
CUI: C0852188
Disease: Necrosis NEC
Necrosis NEC 		1 0 1 5.3E-02 0 0
CUI: C1291610
Disease: Deficiency of mannose-6-phosphate isomerase
Deficiency of mannose-6-phosphate isomerase 		1 0 1 5.3E-02 0 0
CUI: C1844663
Disease: ISLETS OF LANGERHANS, ABSENCE OF
ISLETS OF LANGERHANS, ABSENCE OF 		1 0 1 5.3E-02 0 0
CUI: C1859534
Disease: Bare Lymphocyte Syndrome, Type II, Complementation Group A
Bare Lymphocyte Syndrome, Type II, Complementation Group A 		1 0 1 5.3E-02 0 0
CUI: C1859535
Disease: Bare Lymphocyte Syndrome, Type II, Complementation Group B
Bare Lymphocyte Syndrome, Type II, Complementation Group B 		1 0 1 5.3E-02 0 0
CUI: C1859536
Disease: Bare Lymphocyte Syndrome, Type II, Complementation Group C
Bare Lymphocyte Syndrome, Type II, Complementation Group C 		1 0 1 5.3E-02 0 0
CUI: C1859537
Disease: Bare Lymphocyte Syndrome, Type II, Complementation Group D
Bare Lymphocyte Syndrome, Type II, Complementation Group D 		1 0 1 5.3E-02 0 0
CUI: C1859538
Disease: Bare Lymphocyte Syndrome, Type II, Complementation Group E
Bare Lymphocyte Syndrome, Type II, Complementation Group E 		1 0 1 5.3E-02 0 0
CUI: C1866040
Disease: DIABETES MELLITUS, INSULIN-DEPENDENT, 10
DIABETES MELLITUS, INSULIN-DEPENDENT, 10 		1 0 1 5.3E-02 0 0
CUI: C2609042
Disease: Post embolisation syndrome
Post embolisation syndrome 		1 0 1 5.3E-02 0 0
CUI: C2676498
Disease: BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 (disorder)
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 (disorder) 		1 0 1 5.3E-02 0 0
CUI: C2750471
Disease: COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 8
COLORECTAL CANCER, HEREDITARY NONPOLYPOSIS, TYPE 8 		1 0 1 5.3E-02 0 0
CUI: C3279990
Disease: CANDIDIASIS, FAMILIAL, 7
CANDIDIASIS, FAMILIAL, 7 		1 0 1 5.3E-02 0 0
CUI: C3280501
Disease: INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 1
INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 1 		1 0 1 5.3E-02 0 0
CUI: C3825272
Disease: Food allergy in infants
Food allergy in infants 		1 0 1 5.3E-02 0 0
CUI: C4013950
Disease: IMMUNODEFICIENCY 31A
IMMUNODEFICIENCY 31A 		1 0 1 5.3E-02 0 0
CUI: C4025798
Disease: Abnormalities of placenta or umbilical cord
Abnormalities of placenta or umbilical cord 		1 0 1 5.3E-02 0 0
CUI: C4293676
Disease: Anti-liver cytosolic antigen type 1 antibody positivity
Anti-liver cytosolic antigen type 1 antibody positivity 		1 0 1 5.3E-02 0 0
CUI: C4476942
Disease: Impaired feeding ability
Impaired feeding ability 		1 0 1 5.3E-02 0 0
CUI: C4476964
Disease: Decreased prealbumin level
Decreased prealbumin level 		1 0 1 5.3E-02 0 0
CUI: C4531149
Disease: Reduced proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells
Reduced proportion of CD4-negative, CD8-negative, alpha-beta regulatory T cells 		1 0 1 5.3E-02 0 0