Persistent hyperplastic primary vitreous, autosomal dominant

Preferred Label : Persistent hyperplastic primary vitreous, autosomal dominant;

Symbol : PHPVAD;

CISMeF acronym : PHPVAD;

Type : Phenotype or locus, molecular basis unknown;

Prefixed ID : %611308;

Details

Origin ID

611308;

UMLS CUI

C1969784;

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

Keyword's position in hierarchy(ies) :

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