Iridogoniodysgenesis and skeletal anomalies

Preferred Label : Iridogoniodysgenesis and skeletal anomalies;

Type : Other, mainly phenotypes with suspected mendelian basis;

Prefixed ID : 609515;

Details

Origin ID

609515;

UMLS CUI

C1836074;

Currated CISMeF NLP mapping
- iridogoniodysgenesis and skeletal anomalies [MeSH concept]
- iridogoniodysgenesis and skeletal anomalies [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- iridogoniodysgenesis and skeletal anomalies [MeSH Supplementary Concept]
- iridogoniodysgenesis and skeletal anomalies [MeSH concept]

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