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: C4303860
Disease: Craniofacial ulnar renal syndrome
Craniofacial ulnar renal syndrome 		3 0 3 0.50 0 0
CUI: C0796032
Disease: Malpuech facial clefting syndrome
Malpuech facial clefting syndrome 		4 0 3 0.43 0 0
CUI: C0796059
Disease: Oculopalatoskeletal syndrome
Oculopalatoskeletal syndrome 		2 0 2 0.33 0 0
CUI: C4022490
Disease: Prominent coccyx
Prominent coccyx 		6 0 3 0.33 0 0
CUI: C1861331
Disease: Limited pronation/supination of forearm
Limited pronation/supination of forearm 		7 0 3 0.30 0 0
CUI: C1842563
Disease: Heterotopia, Periventricular, Autosomal Recessive
Heterotopia, Periventricular, Autosomal Recessive 		3 0 2 0.29 0 0
CUI: C4021884
Disease: Bilateral choanal atresia/stenosis
Bilateral choanal atresia/stenosis 		3 0 2 0.29 0 0
CUI: C0796279
Disease: Carnevale syndrome
Carnevale syndrome 		4 0 2 0.25 0 0
CUI: C1303003
Disease: Epicanthus inversus
Epicanthus inversus 		9 0 3 0.25 0 0
CUI: C1832390
Disease: Van Maldergem Wetzburger Verloes syndrome
Van Maldergem Wetzburger Verloes syndrome 		4 0 2 0.25 0 0
CUI: C1849173
Disease: Periventricular gray matter heterotopia
Periventricular gray matter heterotopia 		4 0 2 0.25 0 0
CUI: C0036305
Disease: Schamberg Disease
Schamberg Disease 		6 0 2 0.20 0 0
CUI: C1856765
Disease: Irregular dentition
Irregular dentition 		6 0 2 0.20 0 0
CUI: C3808403
Disease: Large fleshy ears
Large fleshy ears 		13 0 3 0.19 0 0
CUI: C0234244
Disease: Tissue Pain
Tissue Pain 		1 0 1 0.17 0 0
CUI: C0264081
Disease: Osteoarthropathy of fingers familial
Osteoarthropathy of fingers familial 		1 0 1 0.17 0 0
CUI: C0265280
Disease: Spondylometaphyseal dysplasia, Kozlowski type
Spondylometaphyseal dysplasia, Kozlowski type 		1 0 1 0.17 0 0
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism 		1 0 1 0.17 0 0
CUI: C0432227
Disease: Brachyolmia Type 3
Brachyolmia Type 3 		1 0 1 0.17 0 0
CUI: C0562557
Disease: Sexually disinhibited behavior
Sexually disinhibited behavior 		1 0 1 0.17 0 0
CUI: C1838492
Disease: SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder)
SPINAL MUSCULAR ATROPHY, DISTAL, CONGENITAL NONPROGRESSIVE (disorder) 		1 0 1 0.17 0 0
CUI: C1843003
Disease: MITRAL VALVE PROLAPSE, MYXOMATOUS 2
MITRAL VALVE PROLAPSE, MYXOMATOUS 2 		1 0 1 0.17 0 0
CUI: C1847406
Disease: Digital Arthropathy-Brachydactyly, Familial
Digital Arthropathy-Brachydactyly, Familial 		1 0 1 0.17 0 0
CUI: C1847408
Disease: Brachytelomesophalangy
Brachytelomesophalangy 		1 0 1 0.17 0 0
CUI: C1848514
Disease: Short fourth metatarsal
Short fourth metatarsal 		8 0 2 0.17 0 0