Disease #00023 (DFNX-4 (deafness, X-linked, type 4 (DFNX-4)), OMIM:300066)
Official abbreviation |
DFNX-4 |
Name |
deafness, X-linked, type 4 (DFNX-4) |
OMIM ID |
300066 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
SMPX |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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