Disease #02745 (DFNA41 (deafness, autosomal dominant, type 41 (DFNA-41)), OMIM:608224)
Official abbreviation |
DFNA41 |
Name |
deafness, autosomal dominant, type 41 (DFNA-41) |
OMIM ID |
608224 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
P2RX2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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