Hearing loss, profound congenital sensorineural

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Hearing loss, sensorineural, profound congenital [OMIM:Hearing loss, sensorineural, profound congenital]
Sensorineural hearing loss, profound congenital [OMIM:Sensorineural hearing loss, profound congenital]
Quality:
Cross references:
OMIM: "Hearing loss, profound congenital sensorineural" [OMIM:Hearing loss, profound congenital sensorineural]
OMIM: "Hearing loss, sensorineural, profound congenital" [OMIM:Hearing loss, sensorineural, profound congenital]
OMIM: "Sensorineural hearing loss, profound congenital" [OMIM:Sensorineural hearing loss, profound congenital]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

HOMOZYGOUS 11p15-p14 DELETION SYNDROME (OMIM:606528)
USHER SYNDROME, TYPE IC (OMIM:276904)
USHER SYNDROME, TYPE IF (OMIM:602083)