Persistent hyperplastic primary vitreous, autosomal recessive

Preferred Label : Persistent hyperplastic primary vitreous, autosomal recessive;

Obsolete resource : true;

Moved to : 221900;

Prefixed ID : 611311;

Details

Origin ID

611311;

UMLS CUI

C1969783;

Automatic exact mappings (from CISMeF team)
- Persistent hyperplastic primary vitreous [ORDO Disease]
Currated CISMeF NLP mapping
- persistent hyperplastic primary vitreous, autosomal recessive [MeSH concept]
- persistent hyperplastic primary vitreous, autosomal recessive [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- persistent hyperplastic primary vitreous, autosomal recessive [MeSH Supplementary Concept]
- persistent hyperplastic primary vitreous, autosomal recessive [MeSH concept]

Keyword's position in hierarchy(ies) :

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