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: C0157843
Disease: Infective arthritis of shoulder region
Infective arthritis of shoulder region 		1 0 1 0.50 0 0
CUI: C0157844
Disease: Unspecified infective arthritis involving upper arm
Unspecified infective arthritis involving upper arm 		1 0 1 0.50 0 0
CUI: C0157845
Disease: Unspecified infective arthritis involving forearm
Unspecified infective arthritis involving forearm 		1 0 1 0.50 0 0
CUI: C0157846
Disease: Unspecified infective arthritis involving hand
Unspecified infective arthritis involving hand 		1 0 1 0.50 0 0
CUI: C0157847
Disease: Unspecified infective arthritis, pelvic region and thigh
Unspecified infective arthritis, pelvic region and thigh 		1 0 1 0.50 0 0
CUI: C0157848
Disease: Unspecified infective arthritis involving lower leg
Unspecified infective arthritis involving lower leg 		1 0 1 0.50 0 0
CUI: C0157849
Disease: Unspecified infective arthritis, ankle and foot
Unspecified infective arthritis, ankle and foot 		1 0 1 0.50 0 0
CUI: C0162526
Disease: AIDS-Related Opportunistic Infections
AIDS-Related Opportunistic Infections 		1 0 1 0.50 0 0
CUI: C1855758
Disease: Lateral displacement of the femoral head
Lateral displacement of the femoral head 		1 0 1 0.50 0 0
CUI: C3151379
Disease: OKT4 EPITOPE DEFICIENCY
OKT4 EPITOPE DEFICIENCY 		1 0 1 0.50 0 0
CUI: C0020241
Disease: Hydroa Vacciniforme
Hydroa Vacciniforme 		4 0 1 0.20 0 0
CUI: C1504514
Disease: Infection by human herpesvirus 7
Infection by human herpesvirus 7 		4 0 1 0.20 0 0
CUI: C0040458
Disease: Unerupted tooth
Unerupted tooth 		5 0 1 0.17 0 0
CUI: C0339303
Disease: Corneal graft rejection
Corneal graft rejection 		5 0 1 0.17 0 0
CUI: C1855755
Disease: Abnormal immunoglobulin level
Abnormal immunoglobulin level 		6 0 1 0.14 0 0
CUI: C1846582
Disease: Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration 		7 0 1 0.12 0 0
CUI: C1854910
Disease: Shallow acetabular fossae
Shallow acetabular fossae 		8 0 1 0.11 0 0
CUI: C1839254
Disease: Hypoplasia of the capital femoral epiphysis
Hypoplasia of the capital femoral epiphysis 		11 0 1 8.3E-02 0 0
CUI: C3542021
Disease: Duchenne and Becker Muscular Dystrophy
Duchenne and Becker Muscular Dystrophy 		12 0 1 7.7E-02 0 0
CUI: C0586553
Disease: Raised TSH level
Raised TSH level 		13 0 1 7.1E-02 0 0
CUI: C1274233
Disease: T-lymphocyte immunodeficiency
T-lymphocyte immunodeficiency 		15 0 1 6.2E-02 0 0
CUI: C2745959
Disease: Spondyloepiphyseal dysplasia, congenita
Spondyloepiphyseal dysplasia, congenita 		15 0 1 6.2E-02 0 0
CUI: C1846435
Disease: Disproportionate short-trunk short stature
Disproportionate short-trunk short stature 		19 0 1 5.0E-02 0 0
CUI: C0877024
Disease: Schimke immunoosseous dysplasia
Schimke immunoosseous dysplasia 		21 0 1 4.5E-02 0 0
CUI: C1184919
Disease: Thoracic kyphosis
Thoracic kyphosis 		21 0 1 4.5E-02 0 0