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: C0206656
Disease: Embryonal Rhabdomyosarcoma
Embryonal Rhabdomyosarcoma 		121 0 25 0.13 0 0
CUI: C0015923
Disease: Fetal Alcohol Syndrome
Fetal Alcohol Syndrome 		89 0 20 0.12 0 0
CUI: C0278660
Disease: Adult Synovial Sarcoma
Adult Synovial Sarcoma 		198 0 31 0.12 0 0
CUI: C0279982
Disease: Childhood Synovial Sarcoma
Childhood Synovial Sarcoma 		198 0 31 0.12 0 0
CUI: C3714948
Disease: PACHYONYCHIA CONGENITA 3
PACHYONYCHIA CONGENITA 3 		209 0 32 0.12 0 0
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		69 0 17 0.11 0 0
CUI: C0280781
Disease: Adult Pilocytic Astrocytoma
Adult Pilocytic Astrocytoma 		92 0 19 0.11 0 0
CUI: C0280321
Disease: Squamous cell carcinoma of the hypopharynx
Squamous cell carcinoma of the hypopharynx 		103 0 20 0.11 0 0
CUI: C1867441
Disease: Pterygium Of Conjunctiva And Cornea
Pterygium Of Conjunctiva And Cornea 		169 0 26 0.11 0 0
CUI: C4520843
Disease: Pterygium of eye
Pterygium of eye 		169 0 26 0.11 0 0
CUI: C1332995
Disease: Childhood Pilocytic Astrocytoma
Childhood Pilocytic Astrocytoma 		97 0 19 0.11 0 0
CUI: C1962942
Disease: TRICHOMONAS VAGINALIS (finding)
TRICHOMONAS VAGINALIS (finding) 		56 0 15 0.11 0 0
CUI: C0334463
Disease: Malignant Fibrous Histiocytoma
Malignant Fibrous Histiocytoma 		150 0 24 0.11 0 0
CUI: C1266119
Disease: Solitary fibrous tumor
Solitary fibrous tumor 		58 0 15 0.11 0 0
CUI: C0432283
Disease: Osteoglophonic dwarfism
Osteoglophonic dwarfism 		100 0 19 0.11 0 0
CUI: C0686377
Disease: CNS metastases
CNS metastases 		102 0 19 0.10 0 0
CUI: C0206743
Disease: Rhabdoid Tumor
Rhabdoid Tumor 		103 0 19 0.10 0 0
CUI: C1292753
Disease: Primary Effusion Lymphoma
Primary Effusion Lymphoma 		169 0 25 0.10 0 0
CUI: C0032000
Disease: Pituitary Adenoma
Pituitary Adenoma 		170 0 25 0.10 0 0
CUI: C2717836
Disease: Steroid Sulfatase Deficiency Disease
Steroid Sulfatase Deficiency Disease 		181 0 26 0.10 0 0
CUI: C0149939
Disease: Obstructive nephropathy
Obstructive nephropathy 		95 0 18 0.10 0 0
CUI: C1851841
Disease: ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME 1 		129 0 21 0.10 0 0
CUI: C0004565
Disease: Melanoma, B16
Melanoma, B16 		157 0 23 9.9E-02 0 0
CUI: C1260954
Disease: Morphologically altered structure
Morphologically altered structure 		46 0 13 9.8E-02 0 0
CUI: C1512127
Disease: HER2 gene amplification
HER2 gene amplification 		170 0 24 9.8E-02 0 0