iridogoniodysgenesis type1

Preferred Label : iridogoniodysgenesis type1;

MeSH synonym : iridogoniodysgenesis anomaly, autosomal dominant; iridogoniodysgenesis, type 1;

Origin ID

C535535;

UMLS CUI

C1866560;

CISMeF manual mappings
- iridogoniodysgenesis anomaly [Disease (Nov.)]
Currated CISMeF NLP mapping
- Anterior segment developmental anomaly without extraocular manifestations [ORDO Disease]
- Anterior segment dysgenesis 3 [OMIM Phenotype]
- iridogoniodysgenesis syndrome [DO Concept]
MeSH term(s) associated for indexing
- eye abnormalities [MeSH Descriptor]
- glaucoma [MeSH Descriptor]
- iris diseases [MeSH Descriptor]
Record concept(s)
- Iridogoniodysgenesis type1 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]