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: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 0.17 0 0
CUI: C0432269
Disease: Lenz Majewski hyperostotic dwarfism
Lenz Majewski hyperostotic dwarfism 		1 0 1 0.17 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 0.17 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 0.17 0 0
CUI: C1300285
Disease: SAUL-WILSON SYNDROME
SAUL-WILSON SYNDROME 		1 1 1 0.17 1 1.00
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 0.17 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 0.17 0 0
CUI: C1835470
Disease: Progressive sclerosis of skull base
Progressive sclerosis of skull base 		1 0 1 0.17 0 0
CUI: C1837756
Disease: MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY
MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY 		1 0 1 0.17 0 0
CUI: C1837781
Disease: Increased subcutaneous truncal adipose tissue
Increased subcutaneous truncal adipose tissue 		1 0 1 0.17 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 0.17 0 0
CUI: C1861693
Disease: Cervical Vertebral Dysplasia
Cervical Vertebral Dysplasia 		1 0 1 0.17 0 0
CUI: C2675074
Disease: Enlarged peripheral nerve
Enlarged peripheral nerve 		1 0 1 0.17 0 0
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3 		1 0 1 0.17 0 0
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
Progeria Syndrome, Childhood-Onset 		1 0 1 0.17 0 0
CUI: C2750785
Disease: MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) 		1 0 1 0.17 0 0
CUI: C3150736
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj 		1 6 1 0.17 1 0.17
CUI: C3502054
Disease: Leukodystrophy, Dysmyelinating, with Oligodontia
Leukodystrophy, Dysmyelinating, with Oligodontia 		1 0 1 0.17 0 0
CUI: C4016241
Disease: HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL
HUTCHINSON-GILFORD PROGERIA SYNDROME, ATYPICAL 		1 0 1 0.17 0 0
CUI: C4021156
Disease: Enlarged semicircular canal
Enlarged semicircular canal 		1 1 1 0.17 1 1.00
CUI: C4021684
Disease: Sclerosis of hand bone
Sclerosis of hand bone 		1 0 1 0.17 0 0
CUI: C4022125
Disease: Aplasia of the phalanges of the 3rd toe
Aplasia of the phalanges of the 3rd toe 		1 0 1 0.17 0 0
CUI: C4023222
Disease: Abnormal electrophysiology of sinoatrial node origin
Abnormal electrophysiology of sinoatrial node origin 		1 0 1 0.17 0 0
CUI: C4025339
Disease: Abnormality of circulating leptin level
Abnormality of circulating leptin level 		1 0 1 0.17 0 0
CUI: C4025617
Disease: Atlantoaxial abnormality
Atlantoaxial abnormality 		1 0 1 0.17 0 0