| Metadata | |
|---|---|
| ID | DOID:0110832 |
| Name | Usher syndrome type 1F |
| Definition | An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the PCDH15 gene on chromosome 10q. https://www.ncbi.nlm.nih.gov/pubmed/11398101 |
| Xrefs | |
| Synonyms |
USH1F [EXACT] Usher syndrome type IF [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal recessive inheritance |