Disease #02858 (DFNB-23 (deafness, autosomal recessive, type 23 (DFNB-23)), OMIM:609533)
Official abbreviation |
DFNB-23 |
Name |
deafness, autosomal recessive, type 23 (DFNB-23) |
OMIM ID |
609533 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
PCDH15 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
N/A |
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