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: C1735903
Disease: Chronic acidosis
Chronic acidosis 		1 0 1 3.4E-02 0 0
CUI: C1832250
Disease: OBESITY, MODIFIER OF
OBESITY, MODIFIER OF 		1 0 1 3.4E-02 0 0
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF 		1 0 1 3.4E-02 0 0
CUI: C1832253
Disease: INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF 		1 0 1 3.4E-02 0 0
CUI: C1833021
Disease: DEAFNESS, AUTOSOMAL DOMINANT 6
DEAFNESS, AUTOSOMAL DOMINANT 6 		1 0 1 3.4E-02 0 0
CUI: C1833382
Disease: MATURITY-ONSET DIABETES OF THE YOUNG, TYPE IV (disorder)
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE IV (disorder) 		1 0 1 3.4E-02 0 0
CUI: C1835887
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 2 (disorder) 		1 10 1 3.4E-02 7 0.12
CUI: C1838818
Disease: MUSCLE STIFFNESS, PAINFUL
MUSCLE STIFFNESS, PAINFUL 		1 1 1 3.4E-02 1 1.8E-02
CUI: C1840646
Disease: Hepatic Adenomas, Familial
Hepatic Adenomas, Familial 		1 4 1 3.4E-02 3 5.2E-02
CUI: C1849186
Disease: Severe photosensitivity
Severe photosensitivity 		1 0 1 3.4E-02 0 0
CUI: C1852093
Disease: Maturity-Onset Diabetes of the Young, Type 1
Maturity-Onset Diabetes of the Young, Type 1 		1 21 1 3.4E-02 1 1.3E-02
CUI: C1854448
Disease: POLYCYSTIC OVARY SYNDROME, SUSCEPTIBILITY TO
POLYCYSTIC OVARY SYNDROME, SUSCEPTIBILITY TO 		1 1 1 3.4E-02 1 1.8E-02
CUI: C1864623
Disease: DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder)
DIABETES MELLITUS, TRANSIENT NEONATAL, 3 (disorder) 		1 14 1 3.4E-02 1 1.4E-02
CUI: C1864952
Disease: Hyperinsulinemic Hypoglycemia, Familial, 5
Hyperinsulinemic Hypoglycemia, Familial, 5 		1 0 1 3.4E-02 0 0
CUI: C1865290
Disease: Hyperinsulinemic hypoglycemia, familial, 3
Hyperinsulinemic hypoglycemia, familial, 3 		1 10 1 3.4E-02 5 8.1E-02
CUI: C2677132
Disease: MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9 (disorder)
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 9 (disorder) 		1 0 1 3.4E-02 0 0
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		1 122 1 3.4E-02 5 2.9E-02
CUI: C3151466
Disease: HEPATIC LIPASE DEFICIENCY (disorder)
HEPATIC LIPASE DEFICIENCY (disorder) 		1 0 1 3.4E-02 0 0
CUI: C3278384
Disease: HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY
HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY 		1 0 1 3.4E-02 0 0
CUI: C3278636
Disease: Neonatal insulin-dependent diabetes mellitus
Neonatal insulin-dependent diabetes mellitus 		1 0 1 3.4E-02 0 0
CUI: C3280216
Disease: HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3
HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3 		1 0 1 3.4E-02 0 0
CUI: C3280358
Disease: Wolfram-Like Syndrome, Autosomal Dominant
Wolfram-Like Syndrome, Autosomal Dominant 		1 0 1 3.4E-02 0 0
CUI: C3495427
Disease: Fanconi-Bickel Syndrome
Fanconi-Bickel Syndrome 		1 0 1 3.4E-02 0 0
CUI: C3553748
Disease: ADAMS-OLIVER SYNDROME 3
ADAMS-OLIVER SYNDROME 3 		1 5 1 3.4E-02 1 1.6E-02
CUI: C3805412
Disease: CATARACT 41
CATARACT 41 		1 0 1 3.4E-02 0 0