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: C0278511
Disease: Osteosarcoma localised
Osteosarcoma localised 		9 0 4 0.18 0 0
CUI: C0920193
Disease: Photodermatosis
Photodermatosis 		4 0 3 0.17 0 0
CUI: C2044987
Disease: Cervical Glandular Intraepithelial Neoplasia
Cervical Glandular Intraepithelial Neoplasia 		4 0 3 0.17 0 0
CUI: C0332983
Disease: Malassez' epithelial rests
Malassez' epithelial rests 		6 0 3 0.15 0 0
CUI: C1843463
Disease: Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis
Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis 		6 0 3 0.15 0 0
CUI: C1847823
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2F 		6 0 3 0.15 0 0
CUI: C0858009
Disease: Mumps virus infection
Mumps virus infection 		8 0 3 0.14 0 0
CUI: C3711384
Disease: Distal Hereditary Motor Neuropathy, Type II
Distal Hereditary Motor Neuropathy, Type II 		8 0 3 0.14 0 0
CUI: C3697716
Disease: Acute flaccid paralysis
Acute flaccid paralysis 		10 0 3 0.12 0 0
CUI: C3544266
Disease: Hepatobiliary cancer
Hepatobiliary cancer 		11 0 3 0.12 0 0
CUI: C3661519
Disease: Hereditary Motor Neuronopathy
Hereditary Motor Neuronopathy 		12 0 3 0.12 0 0
CUI: C0041182
Disease: Trophoblastic Neoplasms
Trophoblastic Neoplasms 		22 0 4 0.11 0 0
CUI: C0221500
Disease: Effects of heat
Effects of heat 		13 0 3 0.11 0 0
CUI: C2316786
Disease: Chronic kidney disease stage 2
Chronic kidney disease stage 2 		15 0 3 0.10 0 0
CUI: C0271528
Disease: Isosexual precocious puberty
Isosexual precocious puberty 		5 0 2 1.0E-01 0 0
CUI: C1854023
Disease: Spinal muscular atrophy, Jerash type
Spinal muscular atrophy, Jerash type 		5 0 2 1.0E-01 0 0
CUI: C4288754
Disease: Metastatic urothelial carcinoma
Metastatic urothelial carcinoma 		28 0 4 9.8E-02 0 0
CUI: C4509816
Disease: Squamous non-small cell lung cancer
Squamous non-small cell lung cancer 		30 0 4 9.3E-02 0 0
CUI: C1832370
Disease: MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED 		20 0 3 8.8E-02 0 0
CUI: C3899503
Disease: Congenital hypogonadotropic hypogonadism
Congenital hypogonadotropic hypogonadism 		23 0 3 8.1E-02 0 0
CUI: C0042131
Disease: Uterine Diseases
Uterine Diseases 		10 0 2 8.0E-02 0 0
CUI: C4049883
Disease: Obstructive Ureterocele
Obstructive Ureterocele 		25 0 3 7.7E-02 0 0
CUI: C0028643
Disease: Numbness
Numbness 		12 0 2 7.4E-02 0 0
CUI: C0221033
Disease: Trisomy X syndrome
Trisomy X syndrome 		12 0 2 7.4E-02 0 0
CUI: C0270726
Disease: Alexander Disease
Alexander Disease 		27 0 3 7.3E-02 0 0