Disease #06859 (DFNX7 (?Deafness, X-linked 7), OMIM:301018)
Official abbreviation |
DFNX7 |
Name |
?Deafness, X-linked 7 |
OMIM ID |
301018 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
GPRASP2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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