Alacrima, congenital, autosomal dominant

Preferred Label : Alacrima, congenital, autosomal dominant;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Alacrimia congenita, autosomal dominant;

Inheritance : Autosomal dominant;

Prefixed ID : %103420;

Details

Origin ID

103420;

UMLS CUI

C4310836;

Automatic exact mappings (from CISMeF team)
- Agenesis of lacrimal ducts [ICD-11 Sub-sub category]
- Congenital alacrimia [HRDO Sign]
Currated CISMeF NLP mapping
- Congenital alacrima [ORDO Disease]
- alacrima, congenital [MeSH concept]
- alacrima, congenital [MeSH Supplementary Concept]
HPO term(s)
- Alacrima [HPO term]
- Autosomal dominant inheritance [HPO term]
- Decreased lacrimation [HPO term]
- Lacrimal gland hypoplasia [HPO term]
- Lacrimal punctal atresia [HPO term]
- Photophobia [HPO term]
- Punctate corneal epithelial erosions [HPO term]
ORDO concept(s)
- Isolated congenital alacrima [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to BTNT
- Isolated congenital alacrima [ORDO Disease]

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