microphthalmia, isolated, with cataract 1

Preferred Label : microphthalmia, isolated, with cataract 1;

MeSH note : mapped to chromosome 16p13.3;

MeSH synonym : MCOPCT1; cataract, congenital with microphthalmia;

Details

Origin ID

C563582;

UMLS CUI

C1834919;

Currated CISMeF NLP mapping
- Microphthalmia, isolated, with cataract 1 [OMIM Phenotype]
- Microphthalmia-cataract syndrome [ORDO Disease]
MeSH term(s) associated for indexing
- cataract [MeSH Descriptor]
- microphthalmos [MeSH Descriptor]
Record concept(s)
- microphthalmia, isolated, with cataract 1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Microphthalmia, isolated, with cataract 1 [OMIM Phenotype]
- Microphthalmia-cataract syndrome [ORDO Disease]

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