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: C1735903
Disease: Chronic acidosis
Chronic acidosis 		1 0 1 5.0E-02 0 0
CUI: C1835887
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder) 		1 10 1 5.0E-02 6 5.4E-02
CUI: C1840646
Disease: Hepatic Adenomas, Familial
Hepatic Adenomas, Familial 		1 0 1 5.0E-02 0 0
CUI: C1844663
Disease: ISLETS OF LANGERHANS, ABSENCE OF
ISLETS OF LANGERHANS, ABSENCE OF 		1 0 1 5.0E-02 0 0
CUI: C1865290
Disease: Hyperinsulinemic hypoglycemia, familial, 3
Hyperinsulinemic hypoglycemia, familial, 3 		1 11 1 5.0E-02 5 4.4E-02
CUI: C2609269
Disease: Fasting hyperglycaemia
Fasting hyperglycaemia 		1 0 1 5.0E-02 0 0
CUI: C2930809
Disease: Neutropenia and hyperlymphocytosis with large granular lymphocytes
Neutropenia and hyperlymphocytosis with large granular lymphocytes 		1 0 1 5.0E-02 0 0
CUI: C3489795
Disease: Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant 		1 0 1 5.0E-02 0 0
CUI: C3891828
Disease: PANCREATIC AGENESIS 1
PANCREATIC AGENESIS 1 		1 5 1 5.0E-02 4 3.7E-02
CUI: C4014962
Disease: FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THE YOUNG 		1 0 1 5.0E-02 0 0
CUI: C4016117
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET
DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET 		1 0 1 5.0E-02 0 0
CUI: C4021554
Disease: Irregular tarsal ossification
Irregular tarsal ossification 		1 0 1 5.0E-02 0 0
CUI: C4023991
Disease: Ivory epiphyses of the toes
Ivory epiphyses of the toes 		1 0 1 5.0E-02 0 0
CUI: C4025328
Disease: Abnormality of alkaline phosphatase activity
Abnormality of alkaline phosphatase activity 		1 0 1 5.0E-02 0 0
CUI: C4225365
Disease: MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13 		1 5 1 5.0E-02 2 1.8E-02
CUI: C4229700
Disease: Microcephaly (-3 to -9 SD)
Microcephaly (-3 to -9 SD) 		1 0 1 5.0E-02 0 0
CUI: C4274078
Disease: Hyperinsulinism due to HNF4A deficiency
Hyperinsulinism due to HNF4A deficiency 		1 0 1 5.0E-02 0 0
CUI: C4274080
Disease: Autosomal dominant hyperinsulinism due to SUR1 deficiency
Autosomal dominant hyperinsulinism due to SUR1 deficiency 		1 0 1 5.0E-02 0 0
CUI: C4274081
Disease: Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency 		1 0 1 5.0E-02 0 0
CUI: C4288261
Disease: STAT3 Gain of Function
STAT3 Gain of Function 		1 0 1 5.0E-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 5.0E-02 0 0
CUI: C4303475
Disease: Hyperinsulinism due to HNF1A deficiency
Hyperinsulinism due to HNF1A deficiency 		1 0 1 5.0E-02 0 0
CUI: C4476964
Disease: Decreased prealbumin level
Decreased prealbumin level 		1 0 1 5.0E-02 0 0
CUI: C4518822
Disease: 17q12 microdeletion syndrome
17q12 microdeletion syndrome 		1 0 1 5.0E-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 5.0E-02 0 0