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: C1859115
Disease: Prominent interphalangeal joints
Prominent interphalangeal joints 		4 0 2 0.18 0 0
CUI: C1856765
Disease: Irregular dentition
Irregular dentition 		6 0 2 0.15 0 0
CUI: C0559459
Disease: Sacrococcygeal teratoma
Sacrococcygeal teratoma 		7 0 2 0.14 0 0
CUI: C1849311
Disease: Short 1st metacarpal
Short 1st metacarpal 		18 0 3 0.12 0 0
CUI: C0406726
Disease: Orofaciodigital syndrome 3
Orofaciodigital syndrome 3 		1 0 1 0.11 0 0
CUI: C0741918
Disease: Structural cardiac defects
Structural cardiac defects 		1 0 1 0.11 0 0
CUI: C1849164
Disease: Long, smooth philtrum
Long, smooth philtrum 		1 0 1 0.11 0 0
CUI: C1849307
Disease: Increased density of long bones
Increased density of long bones 		1 0 1 0.11 0 0
CUI: C1849309
Disease: Wide distal femoral metaphysis
Wide distal femoral metaphysis 		1 0 1 0.11 0 0
CUI: C1850348
Disease: Hypodysplasia of the corpus callosum
Hypodysplasia of the corpus callosum 		1 0 1 0.11 0 0
CUI: C1851095
Disease: Lumbosacral hirsutism
Lumbosacral hirsutism 		1 0 1 0.11 0 0
CUI: C1855286
Disease: Long curly eyelashes
Long curly eyelashes 		1 0 1 0.11 0 0
CUI: C1861310
Disease: Progressive fusion 2nd-5th pip joints
Progressive fusion 2nd-5th pip joints 		1 0 1 0.11 0 0
CUI: C1861332
Disease: Fusion of midphalangeal joints
Fusion of midphalangeal joints 		1 0 1 0.11 0 0
CUI: C1865241
Disease: Large sternal ossification centers
Large sternal ossification centers 		1 0 1 0.11 0 0
CUI: C1865254
Disease: Distal widening of metacarpals
Distal widening of metacarpals 		1 0 1 0.11 0 0
CUI: C1866657
Disease: Congenital stapes ankylosis
Congenital stapes ankylosis 		1 0 1 0.11 0 0
CUI: C2750805
Disease: Chromosome 5p13 Duplication Syndrome
Chromosome 5p13 Duplication Syndrome 		1 0 1 0.11 0 0
CUI: C3554235
Disease: JOUBERT SYNDROME 20
JOUBERT SYNDROME 20 		1 0 1 0.11 0 0
CUI: C3809352
Disease: MECKEL SYNDROME, TYPE 11
MECKEL SYNDROME, TYPE 11 		1 0 1 0.11 0 0
CUI: C4015141
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 29
MENTAL RETARDATION, AUTOSOMAL DOMINANT 29 		1 0 1 0.11 0 0
CUI: C4015466
Disease: Bilateral clinodactyly
Bilateral clinodactyly 		1 0 1 0.11 0 0
CUI: C4021006
Disease: Short distal phalanx of the 5th toe
Short distal phalanx of the 5th toe 		1 0 1 0.11 0 0
CUI: C4021532
Disease: Abnormality of the stapes
Abnormality of the stapes 		1 0 1 0.11 0 0
CUI: C4022882
Disease: Suprasellar arachnoid cyst
Suprasellar arachnoid cyst 		1 0 1 0.11 0 0