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: C0086395
Disease: Hearing Loss, Extreme
Hearing Loss, Extreme
20 0 20 1.00 0 0
CUI: C0581883
Disease: Complete Hearing Loss
Complete Hearing Loss
20 0 20 1.00 0 0
CUI: C3665473
Disease: Bilateral Deafness
Bilateral Deafness
20 0 20 1.00 0 0
CUI: C4082305
Disease: Deaf Mutism
Deaf Mutism
20 0 20 1.00 0 0
CUI: C0011052
Disease: Prelingual Deafness
Prelingual Deafness
22 0 20 0.91 0 0
CUI: C0011053
Disease: Deafness
Deafness
62 0 20 0.32 0 0
CUI: C0033074
Disease: Presbycusis
Presbycusis
6 0 3 0.13 0 0
CUI: C1860339
Disease: WAARDENBURG SYNDROME, TYPE IIA
WAARDENBURG SYNDROME, TYPE IIA
7 0 3 0.12 0 0
CUI: C4022756
Disease: Profound hearing impairment
Profound hearing impairment
7 0 3 0.12 0 0
Auditory neuropathy spectrum disorder
28 0 5 0.12 0 0
DEAFNESS, AUTOSOMAL RECESSIVE (disorder)
38 0 6 0.12 0 0
CUI: C2700265
Disease: Waardenburg Syndrome Type 2
Waardenburg Syndrome Type 2
9 0 3 0.12 0 0
DEAFNESS, DIGENIC, GJB2/GJB6 (disorder)
3 0 2 9.5E-02 0 0
CUI: C4316813
Disease: Dystopia canthorum
Dystopia canthorum
3 0 2 9.5E-02 0 0
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1
16 0 3 9.1E-02 0 0
DEAFNESS, AUTOSOMAL RECESSIVE 1A (disorder)
4 0 2 9.1E-02 0 0
DEAFNESS, DIGENIC, GJB2/GJB3 (disorder)
4 0 2 9.1E-02 0 0
CUI: C0423318
Disease: Heterochromia iridis
Heterochromia iridis
17 0 3 8.8E-02 0 0
Prelingual sensorineural hearing impairment
17 0 3 8.8E-02 0 0
CUI: C1832828
Disease: Deafness, Autosomal Recessive 9
Deafness, Autosomal Recessive 9
5 0 2 8.7E-02 0 0
CUI: C1836737
Disease: White eyebrow
White eyebrow
7 0 2 8.0E-02 0 0
CUI: C1860344
Disease: Hypoplastic iris stroma
Hypoplastic iris stroma
7 0 2 8.0E-02 0 0
CUI: C3266898
Disease: Waardenburg Syndrome
Waardenburg Syndrome
21 0 3 7.9E-02 0 0
CUI: C1836736
Disease: White eyelashes
White eyelashes
8 0 2 7.7E-02 0 0
CUI: C0392553
Disease: Hereditary peripheral neuropathy
Hereditary peripheral neuropathy
9 0 2 7.4E-02 0 0