| Metadata | |
|---|---|
| ID | DOID:0110841 |
| Name | Usher syndrome type 3A |
| Definition | An Usher syndrome type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the CLRN1 gene on chromosome 3q25. https://www.ncbi.nlm.nih.gov/pubmed/11524702 |
| Xrefs | |
| Synonyms |
USH3A [EXACT] Usher syndrome type IIIA [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal recessive inheritance |