Disease #02810 (DFNB-36 (deafness, autosomal recessive, type 36, with or without vestibular involvement (DFNB-36)), OMIM:609006)
Official abbreviation |
DFNB-36 |
Name |
deafness, autosomal recessive, type 36, with or without vestibular involvement (DFNB-36) |
OMIM ID |
609006 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
ESPN |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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