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: C0456702
Disease: Severe childhood autosomal recessive muscular dystrophy
Severe childhood autosomal recessive muscular dystrophy 		3 0 3 0.21 0 0
CUI: C2936331
Disease: Sarcoglycanopathies
Sarcoglycanopathies 		20 0 6 0.21 0 0
CUI: C2936332
Disease: Alpha-Sarcoglycanopathies
Alpha-Sarcoglycanopathies 		9 0 3 0.15 0 0
CUI: C0267356
Disease: Duodenal perforation
Duodenal perforation 		2 0 2 0.14 0 0
CUI: C1112530
Disease: Leukoplakia of oral mucosa, incl tongue
Leukoplakia of oral mucosa, incl tongue 		2 0 2 0.14 0 0
CUI: C1370932
Disease: carcinoma of the renal pelvis and ureter
carcinoma of the renal pelvis and ureter 		2 0 2 0.14 0 0
CUI: C1540600
Disease: Cerebral seizure
Cerebral seizure 		2 0 2 0.14 0 0
CUI: C1832229
Disease: Rieger syndrome 2 (disorder)
Rieger syndrome 2 (disorder) 		2 0 2 0.14 0 0
CUI: C2675235
Disease: Deafness, Autosomal Recessive 1b
Deafness, Autosomal Recessive 1b 		2 0 2 0.14 0 0
CUI: C4304995
Disease: Recurrent squamous cell carcinoma
Recurrent squamous cell carcinoma 		2 0 2 0.14 0 0
CUI: C0862636
Disease: Adenocarcinoma of the prostate metastatic
Adenocarcinoma of the prostate metastatic 		11 0 3 0.14 0 0
CUI: C0280306
Disease: Verrucous carcinoma of oral cavity
Verrucous carcinoma of oral cavity 		3 0 2 0.13 0 0
CUI: C0339115
Disease: Sebaceous adenocarcinoma of eyelid
Sebaceous adenocarcinoma of eyelid 		3 0 2 0.13 0 0
CUI: C1512431
Disease: High Grade B-Cell Non-Hodgkin's Lymphoma
High Grade B-Cell Non-Hodgkin's Lymphoma 		3 0 2 0.13 0 0
CUI: C2673760
Disease: DEAFNESS, DIGENIC, GJB2/GJB6 (disorder)
DEAFNESS, DIGENIC, GJB2/GJB6 (disorder) 		3 0 2 0.13 0 0
CUI: C2875014
Disease: Acute disseminated encephalitis and encephalomyelitis (ADEM)
Acute disseminated encephalitis and encephalomyelitis (ADEM) 		3 0 2 0.13 0 0
CUI: C3266060
Disease: Botryoid odontogenic cyst
Botryoid odontogenic cyst 		3 0 2 0.13 0 0
CUI: C1263858
Disease: Muscular dystrophy congenital, merosin negative
Muscular dystrophy congenital, merosin negative 		12 0 3 0.13 0 0
CUI: C1456418
Disease: Absence of muscle
Absence of muscle 		12 0 3 0.13 0 0
CUI: C3542021
Disease: Duchenne and Becker Muscular Dystrophy
Duchenne and Becker Muscular Dystrophy 		12 0 3 0.13 0 0
CUI: C0265336
Disease: Senter syndrome
Senter syndrome 		4 0 2 0.12 0 0
CUI: C1844678
Disease: Progressive hearing loss stapes fixation
Progressive hearing loss stapes fixation 		4 0 2 0.12 0 0
CUI: C1861326
Disease: Stapes ankylosis
Stapes ankylosis 		4 0 2 0.12 0 0
CUI: C2673759
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder) 		4 0 2 0.12 0 0
CUI: C2673761
Disease: DEAFNESS, DIGENIC, GJB2/GJB3 (disorder)
DEAFNESS, DIGENIC, GJB2/GJB3 (disorder) 		4 0 2 0.12 0 0