Disease #00021 (DFNX1 (deafness, X-linked, type 1 (DFNX-1)), OMIM:304500)
Official abbreviation |
DFNX1 |
Name |
deafness, X-linked, type 1 (DFNX-1) |
OMIM ID |
304500 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
PRPS1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2012-07-30 11:15:12 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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