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: C4479548
Disease: SPECIFIC GRANULE DEFICIENCY 2
SPECIFIC GRANULE DEFICIENCY 2
2 3 2 0.18 3 0.50
CUI: C4551556
Disease: SPECIFIC GRANULE DEFICIENCY 1
SPECIFIC GRANULE DEFICIENCY 1
2 0 2 0.18 0 0
Recurrent Dedifferentiated Liposarcoma
3 0 2 0.17 0 0
Neutropenia, Severe Congenital, Autosomal Dominant 1
4 0 2 0.15 0 0
CUI: C2931027
Disease: Neutropenia, severe chronic
Neutropenia, severe chronic
6 0 2 0.13 0 0
CUI: C0427543
Disease: Increased blood monocyte number
Increased blood monocyte number
8 0 2 0.12 0 0
CUI: C0743360
Disease: Recurrent ear infections
Recurrent ear infections
11 0 2 1.0E-01 0 0
CUI: C0016479
Disease: Food Poisoning
Food Poisoning
1 0 1 9.1E-02 0 0
CUI: C0241831
Disease: Cerebral salt-wasting syndrome
Cerebral salt-wasting syndrome
1 0 1 9.1E-02 0 0
CUI: C0264356
Disease: Childhood bronchiectasis
Childhood bronchiectasis
1 0 1 9.1E-02 0 0
Derangement of temporomandibular joint
1 0 1 9.1E-02 0 0
CUI: C0277526
Disease: Dysenteric diarrhea
Dysenteric diarrhea
1 0 1 9.1E-02 0 0
CUI: C0333662
Disease: Hemiatrophy
Hemiatrophy
1 0 1 9.1E-02 0 0
CUI: C0343863
Disease: Candida infection of genital region
Candida infection of genital region
1 0 1 9.1E-02 0 0
CUI: C0679360
Disease: Foodborne Disease
Foodborne Disease
1 0 1 9.1E-02 0 0
CUI: C0860029
Disease: Vaginal Yeast Infections
Vaginal Yeast Infections
1 0 1 9.1E-02 0 0
Delayed separation of umbilical cord
1 3 1 9.1E-02 3 0.50
CUI: C1304408
Disease: Urticarial vasculitis
Urticarial vasculitis
1 0 1 9.1E-02 0 0
CUI: C1840013
Disease: Elevated 8-dehydrocholesterol
Elevated 8-dehydrocholesterol
1 0 1 9.1E-02 0 0
CUI: C1840014
Disease: Elevated 8(9)-cholestenol
Elevated 8(9)-cholestenol
1 0 1 9.1E-02 0 0
Stippled calcification in carpal bones
1 0 1 9.1E-02 0 0
CUI: C1844848
Disease: Tarsal stippling
Tarsal stippling
1 0 1 9.1E-02 0 0
Diabetic peripheral neuropathic pain
1 0 1 9.1E-02 0 0
2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic-acid synthase activity
1 0 1 9.1E-02 0 0
Neutropenia, Severe Congenital, Autosomal Dominant 2
1 0 1 9.1E-02 0 0