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: 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
CUI: C3891828
Disease: PANCREATIC AGENESIS 1
PANCREATIC AGENESIS 1 		1 5 1 3.4E-02 1 1.6E-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 1 1 3.4E-02 1 1.8E-02
CUI: C4016117
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET
DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET 		1 0 1 3.4E-02 0 0
CUI: C4016615
Disease: CARDIOMYOPATHY WITH OR WITHOUT SKELETAL MYOPATHY
CARDIOMYOPATHY WITH OR WITHOUT SKELETAL MYOPATHY 		1 0 1 3.4E-02 0 0
CUI: C4016616
Disease: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, PROXIMAL MYOPATHY, AND SUDDEN DEATH
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, PROXIMAL MYOPATHY, AND SUDDEN DEATH 		1 0 1 3.4E-02 0 0
CUI: C4016618
Disease: NEUROPSYCHIATRIC DISORDER AND EARLY-ONSET CATARACT
NEUROPSYCHIATRIC DISORDER AND EARLY-ONSET CATARACT 		1 0 1 3.4E-02 0 0
CUI: C4016735
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF 		1 0 1 3.4E-02 0 0
CUI: C4017627
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, MATERNALLY TRANSMITTED
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MATERNALLY TRANSMITTED 		1 0 1 3.4E-02 0 0
CUI: C4021643
Disease: Impairment of galactose metabolism
Impairment of galactose metabolism 		1 0 1 3.4E-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 3.4E-02 2 3.3E-02
CUI: C4274078
Disease: Hyperinsulinism due to HNF4A deficiency
Hyperinsulinism due to HNF4A deficiency 		1 3 1 3.4E-02 1 1.7E-02
CUI: C4303593
Disease: DEND syndrome
DEND syndrome 		1 0 1 3.4E-02 0 0
CUI: C4551693
Disease: Wolfram Syndrome 1
Wolfram Syndrome 1 		1 0 1 3.4E-02 0 0