retinitis pigmentosa 10
Information
- Disease name
- retinitis pigmentosa 10
- Disease ID
- DOID:0110388
- Description
- "A retinitis pigmentosa that has_material_basis_in mutation in the IMPDH1 gene on chromosome 7q32." [url:https\://www.ncbi.nlm.nih.gov/pubmed/11875050]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:10584
- Cross Reference ID (Disease Ontology)
- ICD10CM:H35.5
- Cross Reference ID (Disease Ontology)
- MESH:C566715
- Cross Reference ID (Disease Ontology)
- MIM:180105
- Exact Synonym (Disease Ontology)
- RP10
- MedGen concept unique identifier (MedGen Concept name)
- C1867299
- MedGen unique identifier (MedGen Concept name)
- 357247