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: C0854297
Disease: Head deformity
Head deformity 		1 0 1 2.0E-02 0 0
CUI: C0859055
Disease: Oedema vascular
Oedema vascular 		1 0 1 2.0E-02 0 0
CUI: C0865474
Disease: Parkinsonism or Parkinson's disease NOS
Parkinsonism or Parkinson's disease NOS 		1 0 1 2.0E-02 0 0
CUI: C0865475
Disease: Idiopathic Parkinsonism or Parkinson's disease
Idiopathic Parkinsonism or Parkinson's disease 		1 0 1 2.0E-02 0 0
CUI: C0865476
Disease: Primary Parkinsonism or Parkinson's disease
Primary Parkinsonism or Parkinson's disease 		1 0 1 2.0E-02 0 0
CUI: C1112341
Disease: Connective tissue inflammation
Connective tissue inflammation 		1 0 1 2.0E-02 0 0
CUI: C1321315
Disease: Paraneoplastic retinopathy
Paraneoplastic retinopathy 		1 0 1 2.0E-02 0 0
CUI: C1321558
Disease: Ocular ischemic syndrome
Ocular ischemic syndrome 		1 0 1 2.0E-02 0 0
CUI: C1510417
Disease: Gait Apraxia
Gait Apraxia 		1 0 1 2.0E-02 0 0
CUI: C1510432
Disease: Radiation Sickness
Radiation Sickness 		1 0 1 2.0E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 2.0E-02 0 0
CUI: C1836474
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 7 		1 6 1 2.0E-02 5 6.7E-02
CUI: C1839332
Disease: Rett Syndrome, Preserved Speech Variant
Rett Syndrome, Preserved Speech Variant 		1 0 1 2.0E-02 0 0
CUI: C1843852
Disease: SPINOCEREBELLAR ATAXIA WITH EPILEPSY
SPINOCEREBELLAR ATAXIA WITH EPILEPSY 		1 0 1 2.0E-02 0 0
CUI: C1844946
Disease: Episodic hypoventilation
Episodic hypoventilation 		1 0 1 2.0E-02 0 0
CUI: C1845336
Disease: AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding)
AUTISM, X-LINKED, SUSCEPTIBILITY TO, 3 (finding) 		1 0 1 2.0E-02 0 0
CUI: C1854182
Disease: PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder)
PARKINSON DISEASE 4, AUTOSOMAL DOMINANT LEWY BODY (disorder) 		1 0 1 2.0E-02 0 0
CUI: C1859863
Disease: Cerebral cortical neurodegeneration
Cerebral cortical neurodegeneration 		1 0 1 2.0E-02 0 0
CUI: C1860972
Disease: GENIOSPASM 1
GENIOSPASM 1 		1 0 1 2.0E-02 0 0
CUI: C1864651
Disease: GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY
GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY 		1 0 1 2.0E-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 2.0E-02 0 0
CUI: C1864670
Disease: Neuronal Ceroid Lipofuscinosis, Congenital
Neuronal Ceroid Lipofuscinosis, Congenital 		1 0 1 2.0E-02 0 0
CUI: C1868595
Disease: PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder) 		1 0 1 2.0E-02 0 0
CUI: C1968550
Disease: Mental Retardation, X-Linked, Syndromic 13
Mental Retardation, X-Linked, Syndromic 13 		1 0 1 2.0E-02 0 0
CUI: C1968551
Disease: Mental Retardation, X-Linked 79
Mental Retardation, X-Linked 79 		1 0 1 2.0E-02 0 0