iridogoniodysgenesis, dominant type

Preferred Label : iridogoniodysgenesis, dominant type;

MeSH synonym : iris hypoplasia with early onset glaucoma, autosomal dominant; iridogoniodysgenesis syndrome; iridogoniodysgenesis type 2; iridogoniodysgenesis, type 2; iris hypoplasia with Early-Onset glaucoma, autosomal dominant;

Détails

Origin ID

C535536;

UMLS CUI

C1842031;

Currated CISMeF NLP mapping
- Anterior segment dysgenesis 4 [OMIM Phenotype]
MeSH term(s) associated for indexing
- anterior chamber [MeSH Descriptor]
- eye abnormalities [MeSH Descriptor]
- glaucoma [MeSH Descriptor]
- iris diseases [MeSH Descriptor]
- tooth abnormalities [MeSH Descriptor]
Record concept(s)
- Iridogoniodysgenesis, dominant type [MeSH concept]
See also inter- (CISMeF)
- iridogoniodysgenesis syndrome [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Anterior segment dysgenesis 4 [OMIM Phenotype]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients