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: C3275445
Disease: X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia 		11 0 1 9.1E-02 0 0
CUI: C4042945
Disease: Severe Acute Malnutrition
Severe Acute Malnutrition 		11 0 1 9.1E-02 0 0
CUI: C0221033
Disease: Trisomy X syndrome
Trisomy X syndrome 		12 0 1 8.3E-02 0 0
CUI: C0334507
Disease: Synovial sarcoma, biphasic
Synovial sarcoma, biphasic 		13 0 1 7.7E-02 0 0
CUI: C0030489
Disease: Paraproteinemias
Paraproteinemias 		14 0 1 7.1E-02 0 0
CUI: C0860218
Disease: ABO incompatibility
ABO incompatibility 		14 0 1 7.1E-02 0 0
CUI: C0017925
Disease: Glycogen Storage Disease Type VI
Glycogen Storage Disease Type VI 		15 0 1 6.7E-02 0 0
CUI: C0862878
Disease: Dedifferentiated chondrosarcoma
Dedifferentiated chondrosarcoma 		15 0 1 6.7E-02 0 0
CUI: C2745959
Disease: Spondyloepiphyseal dysplasia, congenita
Spondyloepiphyseal dysplasia, congenita 		15 0 1 6.7E-02 0 0
CUI: C3840214
Disease: High-functioning autism
High-functioning autism 		15 0 1 6.7E-02 0 0
CUI: C4287594
Disease: Uterine Corpus High Grade Endometrial Stromal Sarcoma
Uterine Corpus High Grade Endometrial Stromal Sarcoma 		15 0 1 6.7E-02 0 0
CUI: C0391861
Disease: Plasma cell inflammation
Plasma cell inflammation 		16 0 1 6.2E-02 0 0
CUI: C0795839
Disease: Chromosome 10, monosomy 10q
Chromosome 10, monosomy 10q 		16 0 1 6.2E-02 0 0
CUI: C0752156
Disease: Dural Arteriovenous Fistula
Dural Arteriovenous Fistula 		17 0 1 5.9E-02 0 0
CUI: C1271398
Disease: Pigment dispersion syndrome (disorder)
Pigment dispersion syndrome (disorder) 		18 0 1 5.6E-02 0 0
CUI: C3541517
Disease: ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT 		18 0 1 5.6E-02 0 0
CUI: C3888065
Disease: ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT 		18 0 1 5.6E-02 0 0
CUI: C0022716
Disease: Menkes Kinky Hair Syndrome
Menkes Kinky Hair Syndrome 		20 0 1 5.0E-02 0 0
CUI: C0553581
Disease: Round cell sarcoma
Round cell sarcoma 		20 0 1 5.0E-02 0 0
CUI: C1868678
Disease: THANATOPHORIC DYSPLASIA, TYPE I (disorder)
THANATOPHORIC DYSPLASIA, TYPE I (disorder) 		20 0 1 5.0E-02 0 0
CUI: C0559260
Disease: Congenital scoliosis
Congenital scoliosis 		21 0 1 4.8E-02 0 0
CUI: C0346326
Disease: Optic Nerve Glioma
Optic Nerve Glioma 		22 0 1 4.5E-02 0 0
CUI: C2242826
Disease: Myeloblastic leukemia
Myeloblastic leukemia 		22 0 1 4.5E-02 0 0
CUI: C0475801
Disease: Leukemia, Prolymphocytic, B-Cell
Leukemia, Prolymphocytic, B-Cell 		23 0 1 4.3E-02 0 0
CUI: C0162568
Disease: Erythropoietic Protoporphyria
Erythropoietic Protoporphyria 		24 0 1 4.2E-02 0 0