hereditary retinal dystrophy
Information
- Disease name
- hereditary retinal dystrophy
- Disease ID
- DOID:8500
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT01920867 | Unknown status | N/A | Stem Cell Ophthalmology Treatment Study | August 2012 | July 2020 |
- Disase is a (Disease Ontology)
- DOID:8501
- Cross Reference ID (Disease Ontology)
- ICD10CM:H35.5
- Cross Reference ID (Disease Ontology)
- ICD9CM:362.7
- Cross Reference ID (Disease Ontology)
- NCI:C35194
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:41799005
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0154860
- MedGen concept unique identifier (MedGen Concept name)
- C0154860
- MedGen unique identifier (MedGen Concept name)
- 57825
- ICD10 preferred id (Insert disease from ICD10)
- D0006170
- ICD10 class code (Insert disease from ICD10)
- H35.5