Disease #05410 (DFNB-68 (deafness, autosomal recessive, type 68 (DFNB-68)), OMIM:610419)
Official abbreviation |
DFNB-68 |
Name |
deafness, autosomal recessive, type 68 (DFNB-68) |
OMIM ID |
610419 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
S1PR2 |
Associated tissues |
- |
Disease features |
autosomal recessive |
Remarks |
- |
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