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 |
- |
Date created |
2014-01-08 19:33:40 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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