Hearing loss, congenital profound

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Hearing loss, congenital, profound (250-8,000 Hz) [OMIM:Hearing loss, congenital, profound (250-8,000 Hz)]
Hearing loss, profound congenital [OMIM:Hearing loss, profound congenital]
Quality:
Cross references:
OMIM: "Hearing loss, congenital profound" [OMIM:Hearing loss, congenital profound]
OMIM: "Hearing loss, congenital, profound (250-8,000 Hz)" [OMIM:Hearing loss, congenital, profound (250-8,000 Hz)]
OMIM: "Hearing loss, profound congenital" [OMIM: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:

DEAFNESS, AUTOSOMAL RECESSIVE 48 (OMIM:609439)
USHER SYNDROME, TYPE ID (OMIM:601067)
USHER SYNDROME, TYPE IG (OMIM:606943)