Disease #00294 (DFNB86 (deafness, nonsyndromic, autosomal recessive, type 86 (DFNB-86)), OMIM:614617)
Official abbreviation |
DFNB86 |
Name |
deafness, nonsyndromic, autosomal recessive, type 86 (DFNB-86) |
OMIM ID |
614617 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
4 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
TBC1D24 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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