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: C0334464
Disease: Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor)
Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor) 		2 0 2 1.00 0 0
CUI: C1707508
Disease: Conventional Dermatofibrosarcoma Protuberans
Conventional Dermatofibrosarcoma Protuberans 		2 0 2 1.00 0 0
CUI: C0334454
Disease: Dermatofibrosarcoma Protuberans, Myxoid
Dermatofibrosarcoma Protuberans, Myxoid 		1 0 1 0.50 0 0
CUI: C0856900
Disease: Sarcoma of skin
Sarcoma of skin 		1 0 1 0.50 0 0
CUI: C1275239
Disease: Dermatomyofibroma
Dermatomyofibroma 		1 0 1 0.50 0 0
CUI: C1394142
Disease: Cortical hyperostosis
Cortical hyperostosis 		1 0 1 0.50 0 0
CUI: C1834345
Disease: Periosteal thickening of long tubular bones
Periosteal thickening of long tubular bones 		1 0 1 0.50 0 0
CUI: C1852924
Disease: OI-EDS Combined Syndrome
OI-EDS Combined Syndrome 		1 0 1 0.50 0 0
CUI: C1859069
Disease: Brittle Bone Disorder
Brittle Bone Disorder 		1 0 1 0.50 0 0
CUI: C3809645
Disease: BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 5 		1 0 1 0.50 0 0
CUI: C3840151
Disease: Congenital glenoid dysplasia
Congenital glenoid dysplasia 		1 0 1 0.50 0 0
CUI: C4015948
Disease: OSTEOGENESIS IMPERFECTA, TYPE III/IV
OSTEOGENESIS IMPERFECTA, TYPE III/IV 		1 0 1 0.50 0 0
CUI: C4015949
Disease: OSTEOGENESIS IMPERFECTA, TYPE IIC
OSTEOGENESIS IMPERFECTA, TYPE IIC 		1 0 1 0.50 0 0
CUI: C4015950
Disease: OSTEOGENESIS IMPERFECTA, TYPE I, MILD
OSTEOGENESIS IMPERFECTA, TYPE I, MILD 		1 0 1 0.50 0 0
CUI: C4015951
Disease: BONE MINERAL DENSITY VARIATION QUANTITATIVE TRAIT LOCUS
BONE MINERAL DENSITY VARIATION QUANTITATIVE TRAIT LOCUS 		1 0 1 0.50 0 0
CUI: C0011330
Disease: Dental Calculus
Dental Calculus 		2 0 1 0.33 0 0
CUI: C0017566
Disease: Gingival Hyperplasia
Gingival Hyperplasia 		2 0 1 0.33 0 0
CUI: C0158713
Disease: Bilateral congenital dislocation of hip
Bilateral congenital dislocation of hip 		2 0 1 0.33 0 0
CUI: C0268345
Disease: EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE
EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE 		2 0 1 0.33 0 0
CUI: C0268360
Disease: Osteogenesis imperfecta, recessive perinatal lethal
Osteogenesis imperfecta, recessive perinatal lethal 		2 0 1 0.33 0 0
CUI: C0334139
Disease: Microglial nodules
Microglial nodules 		2 0 1 0.33 0 0
CUI: C0522205
Disease: Sexual inhibition
Sexual inhibition 		2 0 1 0.33 0 0
CUI: C1833753
Disease: Biconcave flattened vertebrae
Biconcave flattened vertebrae 		2 0 1 0.33 0 0
CUI: C1833754
Disease: Femoral bowing present at birth, straightening with time
Femoral bowing present at birth, straightening with time 		2 0 1 0.33 0 0
CUI: C1851801
Disease: EDS VIIB
EDS VIIB 		2 0 1 0.33 0 0