Stratton-parker syndrome

Preferred Label : Stratton-parker syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Growth hormone deficiency with wormian bones, cardiac anomaly, and brachycamptodactyly;

Prefixed ID : 185120;

Details

Origin ID

185120;

UMLS CUI

C1861448;

Currated CISMeF NLP mapping
- Short stature, wormian bones, dextrocardia syndrome (disorder) [SNOMED CT concept]
- Short stature-wormian bones-dextrocardia syndrome [ORDO Disease]
- Stratton-Parker syndrome [MeSH concept]
- Stratton-Parker syndrome [MeSH Supplementary Concept]
ORDO concept(s)
- Short stature-wormian bones-dextrocardia syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Short stature, wormian bones, dextrocardia syndrome (disorder) [SNOMED CT concept]
- Short stature-wormian bones-dextrocardia syndrome [ORDO Disease]
- Stratton-Parker syndrome [MeSH Supplementary Concept]
- Stratton-Parker syndrome [MeSH concept]

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