cardiocranial syndrome

Preferred Label : cardiocranial syndrome;

MeSH note : Craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis;

MeSH synonym : pfeiffer-type cardiocranial syndrome; pfeiffer syndrome 2; pfeiffer cardiocranial syndrome; pfeiffer singer zschiesche syndrome;

Détails

Origin ID

C535578;

UMLS CUI

C1857495;

Automatic exact mappings (from CISMeF team)
- Pfeiffer syndrome type 2 [ORDO Disease]
- Pfeiffer syndrome type 2 [ICD-11 More detail]
CISMeF manual mappings
- Cardiocranial syndrome Pfeiffer type (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Cardiocranial syndrome, Pfeiffer type [ORDO Disease]
- Craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis [OMIM Phenotype]
MeSH term(s) associated for indexing
- acrocephalosyndactylia [MeSH Descriptor]
- heart defects, congenital [MeSH Descriptor]
Record concept(s)
- Cardiocranial syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cardiocranial syndrome Pfeiffer type (disorder) [SNOMED CT concept]
- Cardiocranial syndrome, Pfeiffer type [ORDO Disease]
- Craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis [OMIM Phenotype]

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