Source: CLINVAR ×
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: C0342276
Disease: Maturity onset diabetes mellitus in young
Maturity onset diabetes mellitus in young 		5 9 5 0.17 2 3.1E-02
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		6 86 4 0.13 13 1.0E-01
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		10 0 4 0.11 0 0
CUI: C1833102
Disease: DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES
DIABETES MELLITUS, PERMANENT NEONATAL, WITH NEUROLOGIC FEATURES 		2 0 2 6.9E-02 0 0
CUI: C1853371
Disease: MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 6 (disorder)
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 6 (disorder) 		2 0 2 6.9E-02 0 0
CUI: C2675071
Disease: HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12
HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12 		2 1 2 6.9E-02 1 1.8E-02
CUI: C2931833
Disease: Hyperinsulinemic hypoglycemia, familial, 2
Hyperinsulinemic hypoglycemia, familial, 2 		2 44 2 6.9E-02 3 3.1E-02
CUI: C3888018
Disease: Congenital Hyperinsulinism
Congenital Hyperinsulinism 		2 10 2 6.9E-02 1 1.5E-02
CUI: C1266042
Disease: Chromophobe Renal Cell Carcinoma
Chromophobe Renal Cell Carcinoma 		3 0 2 6.7E-02 0 0
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism 		4 5 2 6.5E-02 1 1.6E-02
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus 		4 0 2 6.5E-02 0 0
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes 		8 0 2 5.7E-02 0 0
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia 		12 0 2 5.1E-02 0 0
CUI: C0028756
Disease: Obesity, Morbid
Obesity, Morbid 		1 0 1 3.4E-02 0 0
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		1 0 1 3.4E-02 0 0
CUI: C0152164
Disease: Cyclical vomiting syndrome (disorder)
Cyclical vomiting syndrome (disorder) 		1 1 1 3.4E-02 1 1.8E-02
CUI: C0232180
Disease: Cardiac shunt
Cardiac shunt 		1 0 1 3.4E-02 0 0
CUI: C0265344
Disease: Donohue Syndrome
Donohue Syndrome 		1 0 1 3.4E-02 0 0
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		1 1 1 3.4E-02 1 1.8E-02
CUI: C0271695
Disease: Rabson-Mendenhall Syndrome
Rabson-Mendenhall Syndrome 		1 0 1 3.4E-02 0 0
CUI: C0271714
Disease: Hypoglycemia, leucine-induced
Hypoglycemia, leucine-induced 		1 6 1 3.4E-02 5 8.6E-02
CUI: C0342277
Disease: Diabetes mellitus autosomal dominant type II (disorder)
Diabetes mellitus autosomal dominant type II (disorder) 		1 118 1 3.4E-02 5 2.9E-02
CUI: C0342278
Disease: Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans
Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 		1 0 1 3.4E-02 0 0
CUI: C0431693
Disease: Renal cysts and diabetes syndrome
Renal cysts and diabetes syndrome 		1 35 1 3.4E-02 1 1.1E-02
CUI: C0854110
Disease: Insulin-resistant diabetes mellitus
Insulin-resistant diabetes mellitus 		1 0 1 3.4E-02 0 0