persistent hyperplastic primary vitreous, autosomal recessive

Preferred Label : persistent hyperplastic primary vitreous, autosomal recessive;

CISMeF synonym : persistent hyperplastic primary vitreous, autosomal dominant;

Details

Origin ID

C566966;

UMLS CUI

C1969783;

Automatic exact mappings (from CISMeF team)
- Persistent hyperplastic primary vitreous, autosomal dominant [OMIM Phenotype]
- Persistent hyperplastic primary vitreous, autosomal recessive [OMIM Phenotype]
Currated CISMeF NLP mapping
- Persistent hyperplastic primary vitreous, autosomal recessive [OMIM Phenotype]
MeSH term(s) associated for indexing
- eye abnormalities [MeSH Descriptor]
- eye diseases, hereditary [MeSH Descriptor]
Record concept(s)
- persistent hyperplastic primary vitreous, autosomal dominant [MeSH concept]
- persistent hyperplastic primary vitreous, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Persistent hyperplastic primary vitreous, autosomal recessive [OMIM Phenotype]
- Persistent hyperplastic primary vitreous, autosomal recessive [OMIM Phenotype]

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