Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Sensorineural hearing loss, bilateral
117 0 46 0.20 0 0
CUI: C0011053
Disease: Deafness
Deafness
62 0 33 0.17 0 0
Progressive sensorineural hearing impairment
78 28 33 0.16 1 1.1E-02
CUI: C0339789
Disease: Congenital deafness
Congenital deafness
72 11 31 0.15 3 4.1E-02
DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
38 4 25 0.14 1 1.4E-02
CUI: C1384666
Disease: hearing impairment
hearing impairment
740 337 110 0.14 13 3.3E-02
Congenital sensorineural hearing loss
68 0 25 0.12 0 0
Sensorineural Hearing Loss (disorder)
783 111 102 0.12 5 2.9E-02
Nodular Sclerosis Classical Hodgkin Lymphoma
66 22 19 9.0E-02 3 3.5E-02
CUI: C0011052
Disease: Prelingual Deafness
Prelingual Deafness
22 2 14 8.2E-02 1 1.5E-02
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome
68 74 17 7.9E-02 2 1.4E-02
Prelingual sensorineural hearing impairment
17 0 13 7.8E-02 0 0
CUI: C0018780
Disease: Hearing Loss, High-Frequency
Hearing Loss, High-Frequency
35 0 14 7.6E-02 0 0
CUI: C0086395
Disease: Hearing Loss, Extreme
Hearing Loss, Extreme
20 0 12 7.0E-02 0 0
CUI: C0581883
Disease: Complete Hearing Loss
Complete Hearing Loss
20 0 12 7.0E-02 0 0
CUI: C0751068
Disease: Deafness, Acquired
Deafness, Acquired
20 0 12 7.0E-02 0 0
CUI: C3665473
Disease: Bilateral Deafness
Bilateral Deafness
20 0 12 7.0E-02 0 0
CUI: C4082305
Disease: Deaf Mutism
Deaf Mutism
20 0 12 7.0E-02 0 0
CUI: C1848641
Disease: Profound sensorineural hearing loss
Profound sensorineural hearing loss
22 0 12 6.9E-02 0 0
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy
22 0 12 6.9E-02 0 0
Auditory neuropathy spectrum disorder
28 17 12 6.7E-02 1 1.2E-02
CUI: C0859886
Disease: Inherited hearing loss
Inherited hearing loss
13 0 11 6.7E-02 0 0
Severe sensorineural hearing impairment
23 0 11 6.3E-02 0 0
CUI: C0018979
Disease: Hemianopsia
Hemianopsia
41 0 12 6.2E-02 0 0
CUI: C0036454
Disease: Scotoma
Scotoma
21 0 10 5.7E-02 0 0