Microphthalmia, isolated, with cataract 3

Preferred Label : Microphthalmia, isolated, with cataract 3;

Obsolete resource : true;

Moved to : 302200;

Alternative titles and symbols : Mcopct3; Microphthalmia and cataract 3; Cataract, congenital, with microcornea and microphthalmia;

Inheritance : X-linked; Also autosomal dominant and autosomal recessive forms;

Prefixed ID : 302300;

Details

Origin ID

302300;

UMLS CUI

C1844908;

Automatic exact mappings (from CISMeF team)
- Microphthalmia-cataract syndrome [ORDO Disease]
Broader ORDO disease(s)
- Microphthalmia-cataract syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- microphthalmia, isolated, with cataract 3 [MeSH concept]
- microphthalmia, isolated, with cataract 3 [MeSH Supplementary Concept]
ORDO concept(s)
- Microphthalmia-cataract syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- microphthalmia, isolated, with cataract 3 [MeSH Supplementary Concept]
- microphthalmia, isolated, with cataract 3 [MeSH concept]

Keyword's position in hierarchy(ies) :

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