| Metadata | |
|---|---|
| ID | DOID:0110834 |
| Name | Usher syndrome type 1G |
| Definition | An Usher syndrome type 1 that has_material_basis_in caused by homozygous or compound heterozygous mutation in the USH1G gene on chromosome 17q25. https://www.ncbi.nlm.nih.gov/pubmed/12588794 |
| Xrefs | |
| Synonyms |
USH1G [EXACT] Usher syndrome type IG [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some autosomal recessive inheritance |