iridogoniodysgenesis and skeletal anomalies

Preferred Label : iridogoniodysgenesis and skeletal anomalies;

Origin ID

C535534;

UMLS CUI

C1836074;

Currated CISMeF NLP mapping
- Iridogoniodysgenesis and skeletal anomalies [OMIM Phenotype]
MeSH term(s) associated for indexing
- bone and bones [MeSH Descriptor]
- eye abnormalities [MeSH Descriptor]
Record concept(s)
- iridogoniodysgenesis and skeletal anomalies [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Iridogoniodysgenesis and skeletal anomalies [OMIM Phenotype]