| Metadata | |
|---|---|
| ID | DOID:0110386 |
| Name | retinitis pigmentosa 42 |
| Definition | A retinitis pigmentosa that has_material_basis_in mutation in the KLHL7 gene on chromosome 7p15.3. https://www.ncbi.nlm.nih.gov/pubmed/19520207 |
| Xrefs | |
| Synonyms |
RP42 [EXACT] |
| Parent Relationships |
is_a autosomal dominant disease is_a retinitis pigmentosa |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |