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: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 5.0E-02 0 0
CUI: C0393760
Disease: Initial insomnia
Initial insomnia 		1 0 1 5.0E-02 0 0
CUI: C0409635
Disease: Rheumatoid arthritis of ankle
Rheumatoid arthritis of ankle 		1 0 1 5.0E-02 0 0
CUI: C0452143
Disease: Paraplegia, Flaccid
Paraplegia, Flaccid 		1 0 1 5.0E-02 0 0
CUI: C0549618
Disease: MALE GENITAL ABNORMALITIES
MALE GENITAL ABNORMALITIES 		1 0 1 5.0E-02 0 0
CUI: C0744822
Disease: Liver sarcoidosis
Liver sarcoidosis 		1 0 1 5.0E-02 0 0
CUI: C0747195
Disease: pancreatitis biliary
pancreatitis biliary 		1 0 1 5.0E-02 0 0
CUI: C0751761
Disease: Upper Airway Resistance Sleep Apnea Syndrome
Upper Airway Resistance Sleep Apnea Syndrome 		1 0 1 5.0E-02 0 0
CUI: C0853070
Disease: Uterine ischaemia
Uterine ischaemia 		1 0 1 5.0E-02 0 0
CUI: C0854327
Disease: Bacillus infection
Bacillus infection 		1 0 1 5.0E-02 0 0
CUI: C0858613
Disease: Optic nerve oedema
Optic nerve oedema 		1 1 1 5.0E-02 1 5.3E-02
CUI: C0865998
Disease: Segmental Ileitis
Segmental Ileitis 		1 0 1 5.0E-02 0 0
CUI: C0948149
Disease: Splenic Infection
Splenic Infection 		1 0 1 5.0E-02 0 0
CUI: C1136154
Disease: Posterior Tibial Tendon Dysfunction
Posterior Tibial Tendon Dysfunction 		1 0 1 5.0E-02 0 0
CUI: C1142239
Disease: Call-Fleming syndrome
Call-Fleming syndrome 		1 0 1 5.0E-02 0 0
CUI: C1260964
Disease: Eccrine ductal carcinoma
Eccrine ductal carcinoma 		1 0 1 5.0E-02 0 0
CUI: C1332442
Disease: BRCA1 Syndrome
BRCA1 Syndrome 		1 0 1 5.0E-02 0 0
CUI: C1335184
Disease: Ovarian Transitional Cell Carcinoma
Ovarian Transitional Cell Carcinoma 		1 0 1 5.0E-02 0 0
CUI: C1399357
Disease: Hemiparaesthesia
Hemiparaesthesia 		1 0 1 5.0E-02 0 0
CUI: C1832669
Disease: SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) 		1 4 1 5.0E-02 1 4.5E-02
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 5.0E-02 0 0
CUI: C1838457
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP D1
FANCONI ANEMIA, COMPLEMENTATION GROUP D1 		1 0 1 5.0E-02 0 0
CUI: C1850407
Disease: Navajo Familial Neurogenic Arthropathy
Navajo Familial Neurogenic Arthropathy 		1 0 1 5.0E-02 0 0
CUI: C1955566
Disease: Intravenous bisphosphonates
Intravenous bisphosphonates 		1 0 1 5.0E-02 0 0
CUI: C1959600
Disease: Obscure African cardiomyopathy
Obscure African cardiomyopathy 		1 0 1 5.0E-02 0 0