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: C0235328
Disease: Obstruction of colon
Obstruction of colon 		1 0 1 5.3E-02 0 0
CUI: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease 		1 0 1 5.3E-02 0 0
CUI: C0854297
Disease: Head deformity
Head deformity 		1 0 1 5.3E-02 0 0
CUI: C1836474
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7 		1 6 1 5.3E-02 1 0.11
CUI: C1843164
Disease: Charcot-Marie-Tooth disease, demyelinating, Type 1F
Charcot-Marie-Tooth disease, demyelinating, Type 1F 		1 0 1 5.3E-02 0 0
CUI: C1843169
Disease: Clusters of axonal regeneration
Clusters of axonal regeneration 		1 0 1 5.3E-02 0 0
CUI: C1843225
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder) 		1 0 1 5.3E-02 0 0
CUI: C1864669
Disease: NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY
NEURONAL CEROID LIPOFUSCINOSIS DUE TO CATHEPSIN D DEFICIENCY 		1 0 1 5.3E-02 0 0
CUI: C1864670
Disease: Neuronal Ceroid Lipofuscinosis, Congenital
Neuronal Ceroid Lipofuscinosis, Congenital 		1 0 1 5.3E-02 0 0
CUI: C4015371
Disease: MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT
MACULAR DYSTROPHY WITH CENTRAL CONE INVOLVEMENT 		1 0 1 5.3E-02 0 0
CUI: C4016662
Disease: ATAXIA, FRIEDREICH-LIKE, WITH ISOLATED VITAMIN E DEFICIENCY
ATAXIA, FRIEDREICH-LIKE, WITH ISOLATED VITAMIN E DEFICIENCY 		1 0 1 5.3E-02 0 0
CUI: C4016663
Disease: ATAXIA AND RETINITIS PIGMENTOSA WITH ISOLATED VITAMIN E DEFICIENCY
ATAXIA AND RETINITIS PIGMENTOSA WITH ISOLATED VITAMIN E DEFICIENCY 		1 0 1 5.3E-02 0 0
CUI: C4017059
Disease: CEROID LIPOFUSCINOSIS, NEURONAL, 3, PROTRACTED
CEROID LIPOFUSCINOSIS, NEURONAL, 3, PROTRACTED 		1 0 1 5.3E-02 0 0
CUI: C4225283
Disease: DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 7
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 7 		1 0 1 5.3E-02 0 0
CUI: C4225284
Disease: DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 6 		1 0 1 5.3E-02 0 0
CUI: C4285793
Disease: Paroxysmal sympathetic hyperactivity
Paroxysmal sympathetic hyperactivity 		1 0 1 5.3E-02 0 0
CUI: C4310662
Disease: SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 78, AUTOSOMAL RECESSIVE 		1 0 1 5.3E-02 0 0
CUI: C4693509
Disease: CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G 		1 0 1 5.3E-02 0 0
CUI: C4749824
Disease: Charcot-Marie-Tooth disease type 2B5
Charcot-Marie-Tooth disease type 2B5 		1 0 1 5.3E-02 0 0
CUI: C0277827
Disease: Early fontanel closure
Early fontanel closure 		2 0 1 5.0E-02 0 0
CUI: C0752255
Disease: Impairment, Light Touch Sensation
Impairment, Light Touch Sensation 		2 0 1 5.0E-02 0 0
CUI: C0752256
Disease: Pain Sensation Diminished
Pain Sensation Diminished 		2 0 1 5.0E-02 0 0
CUI: C0752257
Disease: Pinprick Sensation Diminished
Pinprick Sensation Diminished 		2 0 1 5.0E-02 0 0
CUI: C0752258
Disease: Position Sense Disorders
Position Sense Disorders 		2 0 1 5.0E-02 0 0
CUI: C0752260
Disease: Proprioceptive Disorders
Proprioceptive Disorders 		2 0 1 5.0E-02 0 0