Microtia with nasolacrimal duct imperforation and eye coloboma

Preferred Label : Microtia with nasolacrimal duct imperforation and eye coloboma;

Type : Phenotype or locus, molecular basis unknown;

Prefixed ID : %611863;

Details

Origin ID

611863;

UMLS CUI

C2678482;

Currated CISMeF NLP mapping
- Microtia, eye coloboma, imperforation of nasolacrimal duct syndrome (disorder) [SNOMED CT concept]
- Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome [ORDO Disease]
- microtia with nasolacrimal duct imperforation and eye coloboma [MeSH concept]
- microtia with nasolacrimal duct imperforation and eye coloboma [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Microtia [HPO term]
ORDO concept(s)
- Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome [ORDO Disease]
- microtia with nasolacrimal duct imperforation and eye coloboma [MeSH Supplementary Concept]
- microtia with nasolacrimal duct imperforation and eye coloboma [MeSH concept]

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