Craniosynostosis

Preferred Label : Craniosynostosis;

Inclusion CIM-10 : Imperfect fusion of skull; Acrocephaly; Trigonocephaly; Oxycephaly;

Diag associé à un acte (%) : 89.4;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q750;

UMLS CUI

C0010278;

Automatic exact mappings (from CISMeF team)
- Acrocephaly (disorder) [SNOMED CT concept]
- Imperfect fusion of skull (disorder) [SNOMED CT concept]
- Isolated oxycephaly [ORDO Disease]
- Oxycephaly [ICD-11 More detail]
- Oxycephaly [HPO term]
- Oxycephaly [MedDRA Preferred Term]
- Trigonocephaly [ICD-11 More detail]
- Trigonocephaly [HPO term]
- Trigonocephaly [PASCAL descriptor]
- Trigonocephaly (disorder) [SNOMED CT concept]
- acrocephaly [MeSH concept]
- craniofacial abnormalities [MedlinePlus Topic]
- msh homeobox 2 [HGNC gene]
- oxycephaly [Radlex concept]
- trigonocephaly [MeSH concept]
Currated CISMeF NLP mapping
- Craniostenosis [HPO term]
- Craniosynostosis [NCIt concept]
- Craniosynostosis [ORDO Disease]
- Craniosynostosis [MedDRA Preferred Term]
- Craniosynostosis [HPO term]
- Craniosynostosis [PASCAL descriptor]
- Craniosynostosis [ACR pathology]
- Craniosynostosis [ICD-10 Sub-category (who)]
- Craniosynostosis [ICD-11 Subcategory]
- Craniosynostosis [OMIM phenotypic series]
- Craniosynostosis (coronal, sagittal, lambdoid sutures) [HPO term]
- Craniosynostosis syndrome (disorder) [SNOMED CT concept]
- Craniosynostosis, coronal and lambdoidal [HPO term]
- craniosynostoses [MeSH concept]
- craniosynostoses [MeSH Descriptor]
- craniosynostosis [Radlex concept]
- craniosynostosis [Disease (Nov.)]
- craniosynostosis [DO Concept]
- craniosynostosis syndrome [SNOMED Notion]
- premature closure of cranial sutures [MedDRA Preferred Term]
DO Cross reference
- craniosynostosis [DO Concept]
Manual NTBT mappings (CISMeF)
- Syndromic craniosynostosis [ORDO Disease]
Orphanet concepts
- Baller-Gerold syndrome [ORDO Disease]
- Craniosynostosis [ORDO Disease]
- Craniosynostosis, Herrmann-Opitz type [ORDO Disease]
- Familial lambdoid synostosis [ORDO Disease]
- Familial scaphocephaly syndrome [ORDO Disease]
- Isolated cloverleaf skull syndrome [ORDO Disease]
- Isolated oxycephaly [ORDO Disease]
- Non-syndromic bicoronal craniosynostosis [ORDO Disease]
- Non-syndromic craniosynostosis [ORDO Disease]
- Non-syndromic metopic craniosynostosis [ORDO Disease]
- Non-syndromic sagittal craniosynostosis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Craniostenosis [HPO term]
- Craniosynostosis [MedDRA Preferred Term]
- Craniosynostosis [ACR pathology]
- Craniosynostosis [HPO term]
- Craniosynostosis [NCIt concept]
- Craniosynostosis [ORDO Disease]
- Craniosynostosis [PASCAL descriptor]
- Craniosynostosis (coronal, sagittal, lambdoid sutures) [HPO term]
- Craniosynostosis 1 [OMIM Phenotype]
- Craniosynostosis syndrome (disorder) [SNOMED CT concept]
- Craniosynostosis, coronal and lambdoidal [HPO term]
- Non-syndromic craniosynostosis [ORDO Disease]
- Premature closure of cranial sutures [MedDRA LLT]
- craniosynostoses [MeSH Descriptor]
- craniosynostoses [MeSH concept]
- craniosynostosis [Radlex concept]
- craniosynostosis [DO Concept]
- craniosynostosis [Disease (Nov.)]
- craniosynostosis syndrome [SNOMED Notion]
- premature closure of cranial sutures [MedDRA Preferred Term]
Validated automatic mappings to BTNT
- Craniosynostosis 1 [OMIM Phenotype]
- Non-syndromic craniosynostosis [ORDO Disease]

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