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: C0454592
Disease: Deep dyslexia
Deep dyslexia 		1 0 1 6.9E-03 0 0
CUI: C0495694
Disease: Dysarthria and anarthria
Dysarthria and anarthria 		1 0 1 6.9E-03 0 0
CUI: C0524679
Disease: Neuropapillitis
Neuropapillitis 		1 0 1 6.9E-03 0 0
CUI: C0559523
Disease: Genital tuberculosis
Genital tuberculosis 		1 0 1 6.9E-03 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 6.9E-03 0 0
CUI: C0730309
Disease: Inherited optic neuropathy
Inherited optic neuropathy 		1 0 1 6.9E-03 0 0
CUI: C0796019
Disease: SPASTIC PARAPLEGIA 23 (disorder)
SPASTIC PARAPLEGIA 23 (disorder) 		1 0 1 6.9E-03 0 0
CUI: C0796036
Disease: Marinesco-Sjogren-like syndrome (MSLS)
Marinesco-Sjogren-like syndrome (MSLS) 		1 0 1 6.9E-03 0 0
CUI: C0796124
Disease: Proud Syndrome
Proud Syndrome 		1 0 1 6.9E-03 0 0
CUI: C0796159
Disease: Mental retardation Smith Fineman Myers type
Mental retardation Smith Fineman Myers type 		1 0 1 6.9E-03 0 0
CUI: C0854963
Disease: Metastatic Penile Cancer
Metastatic Penile Cancer 		1 0 1 6.9E-03 0 0
CUI: C0862793
Disease: Adenocarcinoma of lung stage IIIB
Adenocarcinoma of lung stage IIIB 		1 0 1 6.9E-03 0 0
CUI: C0948075
Disease: Anal infection
Anal infection 		1 0 1 6.9E-03 0 0
CUI: C1275155
Disease: Multiple basal cell papillomata
Multiple basal cell papillomata 		1 0 1 6.9E-03 0 0
CUI: C1336109
Disease: Stage IA1 Cervical Cancer
Stage IA1 Cervical Cancer 		1 0 1 6.9E-03 0 0
CUI: C1367859
Disease: Pineal parenchymal tumor of intermediate differentiation
Pineal parenchymal tumor of intermediate differentiation 		1 0 1 6.9E-03 0 0
CUI: C1456275
Disease: Mitochondrial metabolism disorder, unspecified
Mitochondrial metabolism disorder, unspecified 		1 0 1 6.9E-03 0 0
CUI: C1515286
Disease: Testicular Intratubular Germ Cell Neoplasia, Unclassified
Testicular Intratubular Germ Cell Neoplasia, Unclassified 		1 0 1 6.9E-03 0 0
CUI: C1711276
Disease: carcinosarcoma of lung
carcinosarcoma of lung 		1 0 1 6.9E-03 0 0
CUI: C1719528
Disease: Other stomatitis and mucositis (ulcerative)
Other stomatitis and mucositis (ulcerative) 		1 0 1 6.9E-03 0 0
CUI: C1735375
Disease: Progressive optic neuropathy
Progressive optic neuropathy 		1 0 1 6.9E-03 0 0
CUI: C1832669
Disease: SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 9, AUTOSOMAL DOMINANT (disorder) 		1 0 1 6.9E-03 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 6.9E-03 0 0
CUI: C1835826
Disease: Renal Hypodysplasia, Nonsyndromic, 1
Renal Hypodysplasia, Nonsyndromic, 1 		1 0 1 6.9E-03 0 0
CUI: C1835851
Disease: Ichthyosis with hypotrichosis, autosomal recessive
Ichthyosis with hypotrichosis, autosomal recessive 		1 0 1 6.9E-03 0 0