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: C4015948
Disease: OSTEOGENESIS IMPERFECTA, TYPE III/IV
OSTEOGENESIS IMPERFECTA, TYPE III/IV 		1 0 1 0.20 0 0
CUI: C4015949
Disease: OSTEOGENESIS IMPERFECTA, TYPE IIC
OSTEOGENESIS IMPERFECTA, TYPE IIC 		1 0 1 0.20 0 0
CUI: C4015950
Disease: OSTEOGENESIS IMPERFECTA, TYPE I, MILD
OSTEOGENESIS IMPERFECTA, TYPE I, MILD 		1 0 1 0.20 0 0
CUI: C4015951
Disease: BONE MINERAL DENSITY VARIATION QUANTITATIVE TRAIT LOCUS
BONE MINERAL DENSITY VARIATION QUANTITATIVE TRAIT LOCUS 		1 0 1 0.20 0 0
CUI: C4268640
Disease: Mixed irritable bowel syndrome
Mixed irritable bowel syndrome 		1 0 1 0.20 0 0
CUI: C4303789
Disease: Ehlers-Danlos syndrome cardiac valvular type
Ehlers-Danlos syndrome cardiac valvular type 		1 0 1 0.20 0 0
CUI: C4310978
Disease: EHLERS-DANLOS/OSTEOGENESIS IMPERFECTA CROSSOVER SYNDROME
EHLERS-DANLOS/OSTEOGENESIS IMPERFECTA CROSSOVER SYNDROME 		1 0 1 0.20 0 0
CUI: C0268358
Disease: Osteogenesis imperfecta, dominant perinatal lethal
Osteogenesis imperfecta, dominant perinatal lethal 		8 0 2 0.18 0 0
CUI: C0011330
Disease: Dental Calculus
Dental Calculus 		2 0 1 0.17 0 0
CUI: C0014571
Disease: Epiphyses, Slipped
Epiphyses, Slipped 		2 0 1 0.17 0 0
CUI: C0158713
Disease: Bilateral congenital dislocation of hip
Bilateral congenital dislocation of hip 		2 0 1 0.17 0 0
CUI: C0334464
Disease: Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor)
Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor) 		2 0 1 0.17 0 0
CUI: C0410787
Disease: Hereditary Connective Tissue Disorder
Hereditary Connective Tissue Disorder 		9 0 2 0.17 0 0
CUI: C0542428
Disease: Hypochondrogenesis
Hypochondrogenesis 		2 0 1 0.17 0 0
CUI: C1707508
Disease: Conventional Dermatofibrosarcoma Protuberans
Conventional Dermatofibrosarcoma Protuberans 		2 0 1 0.17 0 0
CUI: C2931280
Disease: Perniola Krajewska Carnevale syndrome
Perniola Krajewska Carnevale syndrome 		2 0 1 0.17 0 0
CUI: C4025145
Disease: Cortical irregularity
Cortical irregularity 		2 0 1 0.17 0 0
CUI: C4551986
Disease: AMR Syndrome
AMR Syndrome 		2 0 1 0.17 0 0
CUI: C4707450
Disease: Ring chromosome 5 syndrome
Ring chromosome 5 syndrome 		2 0 1 0.17 0 0
CUI: C0409495
Disease: Protrusio acetabuli
Protrusio acetabuli 		10 0 2 0.15 0 0
CUI: C1833762
Disease: Decreased calvarial ossification
Decreased calvarial ossification 		10 0 2 0.15 0 0
CUI: C0152093
Disease: Hypermobility syndrome
Hypermobility syndrome 		3 0 1 0.14 0 0
CUI: C0220679
Disease: Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified
Ehlers-Danlos Syndrome, Autosomal Dominant, Type Unspecified 		3 0 1 0.14 0 0
CUI: C0220685
Disease: Achondrogenesis type 2
Achondrogenesis type 2 		3 0 1 0.14 0 0
CUI: C0263664
Disease: Generalized morphea
Generalized morphea 		3 0 1 0.14 0 0