Microphthalmia/coloboma 2

Preferred Label : Microphthalmia/coloboma 2;

Symbol : MCOPCB2;

CISMeF acronym : MCOPCB2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Microphthalmia, colobomatous, 2; MCOPCB2;

Description : For a discussion of genetic heterogeneity of isolated colobomatous microphthalmia, see MCOPCB1 (300345).;

Prefixed ID : %605738;

Details

Origin ID

605738;

UMLS CUI

C1854018;

Broader ORDO disease(s)
- Colobomatous microphthalmia [ORDO Disease]
Currated CISMeF NLP mapping
- microphthalmia, isolated, with coloboma 2 [MeSH concept]
- microphthalmia, isolated, with coloboma 2 [MeSH Supplementary Concept]
ORDO concept(s)
- Colobomatous microphthalmia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- microphthalmia, isolated, with coloboma 2 [MeSH Supplementary Concept]
- microphthalmia, isolated, with coloboma 2 [MeSH concept]
Validated automatic mappings to NTBT
- Colobomatous microphthalmia [ORDO Disease]

Keyword's position in hierarchy(ies) :

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