Source: INFERRED ×
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: C0033300
Disease: Progeria
Progeria 		1 20 1 0.12 1 2.9E-02
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 0.12 0 0
CUI: C0079035
Disease: Bradyarrhythmia (disorder)
Bradyarrhythmia (disorder) 		1 0 1 0.12 0 0
CUI: C0342277
Disease: Diabetes mellitus autosomal dominant type II (disorder)
Diabetes mellitus autosomal dominant type II (disorder) 		1 118 1 0.12 3 2.3E-02
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss 		1 0 1 0.12 0 0
CUI: C0410190
Disease: Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder) 		1 25 1 0.12 1 2.6E-02
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis 		1 8 1 0.12 1 4.5E-02
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 4 1 0.12 1 5.6E-02
CUI: C1720860
Disease: Familial Partial Lipodystrophy, Type 2
Familial Partial Lipodystrophy, Type 2 		1 17 1 0.12 2 6.7E-02
CUI: C1834653
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder)
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder) 		1 0 1 0.12 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 0.12 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 0.12 0 0
CUI: C1840646
Disease: Hepatic Adenomas, Familial
Hepatic Adenomas, Familial 		1 0 1 0.12 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 3 1 0.12 1 5.9E-02
CUI: C1865290
Disease: Hyperinsulinemic hypoglycemia, familial, 3
Hyperinsulinemic hypoglycemia, familial, 3 		1 0 1 0.12 0 0
CUI: C2675074
Disease: Enlarged peripheral nerve
Enlarged peripheral nerve 		1 0 1 0.12 0 0
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3 		1 4 1 0.12 1 5.6E-02
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
Progeria Syndrome, Childhood-Onset 		1 0 1 0.12 0 0
CUI: C2750785
Disease: MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) 		1 13 1 0.12 1 3.7E-02
CUI: C4016117
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET
DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET 		1 0 1 0.12 0 0
CUI: C4016241
Disease: HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL
HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL 		1 0 1 0.12 0 0
CUI: C4021684
Disease: Sclerosis of hand bone
Sclerosis of hand bone 		1 0 1 0.12 0 0
CUI: C4022125
Disease: Aplasia of the phalanges of the 3rd toe
Aplasia of the phalanges of the 3rd toe 		1 0 1 0.12 0 0
CUI: C4023222
Disease: Abnormal electrophysiology of sinoatrial node origin
Abnormal electrophysiology of sinoatrial node origin 		1 0 1 0.12 0 0
CUI: C4025339
Disease: Abnormality of circulating leptin level
Abnormality of circulating leptin level 		1 0 1 0.12 0 0