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: C0015708
Disease: Fazio-Londe Syndrome
Fazio-Londe Syndrome 		1 0 1 3.1E-02 0 0
CUI: C0234505
Disease: Tactile Agnosia
Tactile Agnosia 		1 0 1 3.1E-02 0 0
CUI: C0235910
Disease: Colagenosis
Colagenosis 		1 0 1 3.1E-02 0 0
CUI: C0242036
Disease: Paraplegia, Ataxic
Paraplegia, Ataxic 		1 0 1 3.1E-02 0 0
CUI: C0270804
Disease: Spastic Diplegia Cerebral Palsy
Spastic Diplegia Cerebral Palsy 		1 0 1 3.1E-02 0 0
CUI: C0278114
Disease: Paraplegia, Cerebral
Paraplegia, Cerebral 		1 0 1 3.1E-02 0 0
CUI: C0278115
Disease: Paraplegia, Spinal
Paraplegia, Spinal 		1 0 1 3.1E-02 0 0
CUI: C0393540
Disease: Childhood Progressive Bulbar Palsy
Childhood Progressive Bulbar Palsy 		1 0 1 3.1E-02 0 0
CUI: C0452143
Disease: Paraplegia, Flaccid
Paraplegia, Flaccid 		1 0 1 3.1E-02 0 0
CUI: C0495694
Disease: Dysarthria and anarthria
Dysarthria and anarthria 		1 0 1 3.1E-02 0 0
CUI: C0524679
Disease: Neuropapillitis
Neuropapillitis 		1 0 1 3.1E-02 0 0
CUI: C0685874
Disease: Congenital abnormal shape of inner ear
Congenital abnormal shape of inner ear 		1 0 1 3.1E-02 0 0
CUI: C0796036
Disease: Marinesco-Sjogren-like syndrome (MSLS)
Marinesco-Sjogren-like syndrome (MSLS) 		1 0 1 3.1E-02 0 0
CUI: C1328618
Disease: Agraphesthesia
Agraphesthesia 		1 0 1 3.1E-02 0 0
CUI: C1835896
Disease: SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder)
SPASTIC PARAPLEGIA 30, AUTOSOMAL RECESSIVE (disorder) 		1 0 1 3.1E-02 0 0
CUI: C1839564
Disease: Jensen syndrome
Jensen syndrome 		1 0 1 3.1E-02 0 0
CUI: C1843014
Disease: Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Unusual Plaques 		1 0 1 3.1E-02 0 0
CUI: C1843015
Disease: Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia
Alzheimer Disease, Familial, 3, with Spastic Paraparesis and Apraxia 		1 0 1 3.1E-02 0 0
CUI: C1844836
Disease: Ayazi syndrome
Ayazi syndrome 		1 0 1 3.1E-02 0 0
CUI: C1845543
Disease: Mental Retardation, X-Linked, with Epilepsy
Mental Retardation, X-Linked, with Epilepsy 		1 0 1 3.1E-02 0 0
CUI: C1848735
Disease: Developmental delay, mild
Developmental delay, mild 		1 0 1 3.1E-02 0 0
CUI: C1853251
Disease: Spastic Paraplegia 33, Autosomal Dominant
Spastic Paraplegia 33, Autosomal Dominant 		1 0 1 3.1E-02 0 0
CUI: C1864929
Disease: Cerebellar atrophy, progressive
Cerebellar atrophy, progressive 		1 0 1 3.1E-02 0 0
CUI: C1865864
Disease: AMYOTROPHIC LATERAL SCLEROSIS 5
AMYOTROPHIC LATERAL SCLEROSIS 5 		1 0 1 3.1E-02 0 0
CUI: C1955871
Disease: Cobblestone Complex
Cobblestone Complex 		1 0 1 3.1E-02 0 0