Retinal dysplasia, primary

Preferred Label : Retinal dysplasia, primary;

Symbol : PRD;

CISMeF acronym : PRD;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : X-linked; ? same as retinoschisis; ? allelic to Norrie disease;

Prefixed ID : 312550;

Details

Origin ID

312550;

UMLS CUI

C3887971;

Currated CISMeF NLP mapping
- X-linked retinal dysplasia [ORDO Disease]
- X-linked retinal dysplasia (disorder) [SNOMED CT concept]
HPO term(s)
- Falciform retinal fold [HPO term]
- Retinal dysplasia [HPO term]
- X-linked inheritance [HPO term]
ORDO concept(s)
- X-linked retinal dysplasia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients