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: C0238707
Disease: Impairment of attention
Impairment of attention 		5 0 3 0.12 0 0
CUI: C0206586
Disease: Endolymphatic Hydrops
Endolymphatic Hydrops 		11 0 3 1.0E-01 0 0
CUI: C1395088
Disease: Nervous system--Degeneration
Nervous system--Degeneration 		4 0 2 8.3E-02 0 0
CUI: C3711380
Disease: Huntington Disease-Like Syndrome
Huntington Disease-Like Syndrome 		6 0 2 7.7E-02 0 0
CUI: C0339534
Disease: Usher syndrome type 2
Usher syndrome type 2 		8 0 2 7.1E-02 0 0
CUI: C4284088
Disease: MIRAGE SYNDROME
MIRAGE SYNDROME 		8 0 2 7.1E-02 0 0
CUI: C1963674
Disease: Spinocerebellar Ataxia 10
Spinocerebellar Ataxia 10 		9 0 2 6.9E-02 0 0
CUI: C0677501
Disease: Congenital Nephrogenic Diabetes Insipidus
Congenital Nephrogenic Diabetes Insipidus 		11 0 2 6.5E-02 0 0
CUI: C1955603
Disease: Deaf-Blind Disorders
Deaf-Blind Disorders 		11 0 2 6.5E-02 0 0
CUI: C4023551
Disease: Abnormality of dental color
Abnormality of dental color 		11 0 2 6.5E-02 0 0
CUI: C1568249
Disease: Usher Syndrome, Type II
Usher Syndrome, Type II 		12 0 2 6.2E-02 0 0
CUI: C0240341
Disease: Micrographia
Micrographia 		14 0 2 5.9E-02 0 0
CUI: C1997740
Disease: Segmental dystonia
Segmental dystonia 		15 0 2 5.7E-02 0 0
CUI: C0432284
Disease: Infantile myofibromatosis
Infantile myofibromatosis 		18 0 2 5.3E-02 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2 		18 0 2 5.3E-02 0 0
CUI: C0010232
Disease: Cowpox
Cowpox 		19 0 2 5.1E-02 0 0
CUI: C0206648
Disease: Myofibromatosis
Myofibromatosis 		19 0 2 5.1E-02 0 0
CUI: C0393534
Disease: Paraneoplastic Cerebellar Degeneration
Paraneoplastic Cerebellar Degeneration 		19 0 2 5.1E-02 0 0
CUI: C4551520
Disease: Intention tremor
Intention tremor 		20 0 2 5.0E-02 0 0
CUI: C0036454
Disease: Scotoma
Scotoma 		21 0 2 4.9E-02 0 0
CUI: C0267071
Disease: Oropharyngeal Dysphagia
Oropharyngeal Dysphagia 		43 0 3 4.8E-02 0 0
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy 		22 0 2 4.8E-02 0 0
CUI: C0263628
Disease: Tumoral calcinosis
Tumoral calcinosis 		45 0 3 4.7E-02 0 0
CUI: C0018121
Disease: Gradenigo Syndrome
Gradenigo Syndrome 		1 0 1 4.5E-02 0 0
CUI: C0026686
Disease: Mucocele of salivary gland
Mucocele of salivary gland 		1 0 1 4.5E-02 0 0