Craniosynostosis, philadelphia type

Preferred Label : Craniosynostosis, philadelphia type;

Obsolete resource : true;

Moved to : 185900;

Inheritance : Autosomal dominant;

Prefixed ID : 601222;

Details

Origin ID

601222;

UMLS CUI

C1832590;

Currated CISMeF NLP mapping
- Craniosynostosis Philadelphia type (disorder) [SNOMED CT concept]
- Craniosynostosis, Philadelphia type [ICD-11 More detail]
- Craniosynostosis, Philadelphia type [ORDO Disease]
- craniosynostosis, philadelphia type [MeSH concept]
- craniosynostosis, philadelphia type [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Craniosynostosis Philadelphia type (disorder) [SNOMED CT concept]
- Craniosynostosis, Philadelphia type [ORDO Disease]
- craniosynostosis, philadelphia type [MeSH Supplementary Concept]
- craniosynostosis, philadelphia type [MeSH concept]

Keyword's position in hierarchy(ies) :

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