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: C0011052
Disease: Prelingual Deafness
Prelingual Deafness
22 0 22 0.35 0 0
CUI: C0086395
Disease: Hearing Loss, Extreme
Hearing Loss, Extreme
20 0 20 0.32 0 0
CUI: C0581883
Disease: Complete Hearing Loss
Complete Hearing Loss
20 0 20 0.32 0 0
CUI: C0751068
Disease: Deafness, Acquired
Deafness, Acquired
20 0 20 0.32 0 0
CUI: C3665473
Disease: Bilateral Deafness
Bilateral Deafness
20 0 20 0.32 0 0
CUI: C4082305
Disease: Deaf Mutism
Deaf Mutism
20 0 20 0.32 0 0
CUI: C0339789
Disease: Congenital deafness
Congenital deafness
72 0 21 0.19 0 0
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness
163 0 33 0.17 0 0
DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
38 0 14 0.16 0 0
Congenital sensorineural hearing loss
68 17 16 0.14 1 1.9E-02
Sensorineural hearing loss, bilateral
117 0 21 0.13 0 0
Prelingual sensorineural hearing impairment
17 0 9 0.13 0 0
CUI: C3887873
Disease: Hearing Loss
Hearing Loss
18 0 9 0.13 0 0
Nodular Sclerosis Classical Hodgkin Lymphoma
66 0 13 0.11 0 0
Progressive sensorineural hearing impairment
78 0 14 0.11 0 0
Auditory neuropathy spectrum disorder
28 0 9 0.11 0 0
CUI: C0018780
Disease: Hearing Loss, High-Frequency
Hearing Loss, High-Frequency
35 0 9 0.10 0 0
CUI: C1843865
Disease: Vestibular dysfunction
Vestibular dysfunction
16 0 7 9.9E-02 0 0
CUI: C1852271
Disease: Auditory neuropathy
Auditory neuropathy
24 0 7 8.9E-02 0 0
CUI: C0859886
Disease: Inherited hearing loss
Inherited hearing loss
13 0 6 8.7E-02 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome
68 0 10 8.3E-02 0 0
CUI: C4022756
Disease: Profound hearing impairment
Profound hearing impairment
7 0 5 7.8E-02 0 0
CUI: C0036454
Disease: Scotoma
Scotoma
21 0 6 7.8E-02 0 0
CUI: C1848641
Disease: Profound sensorineural hearing loss
Profound sensorineural hearing loss
22 0 6 7.7E-02 0 0
CUI: C4023018
Disease: Subcortical cerebral atrophy
Subcortical cerebral atrophy
22 0 6 7.7E-02 0 0