Disease #02908 (DFNB49 (deafness, autosomal recessive, type 49 (DFNB-49)), OMIM:610153)
| Official abbreviation |
DFNB49 |
| Name |
deafness, autosomal recessive, type 49 (DFNB-49) |
| OMIM ID |
610153 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
MARVELD2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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