Autosomal recessive nonsyndromic hearing loss 39
Autosomal recessive nonsyndromic hearing loss 39
Definition
An autosomal recessive disorder caused by mutations in the HGF gene, encoding hepatocyte growth factor receptor. It is characterized by profound deafness.
Also known as autosomal recessive nonsyndromic hearing loss 39 — per MONDO
Also identified as
- DOID 0110497 per MONDO
- MESH C564265 per MONDO
- NCIT C129874 per MONDO
- OMIM 608265 per MONDO
- UMLS C1842342 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Craniocervical region | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Craniocervical region | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Ear | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Ear | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |