craniosynostoses

Preferred Label : craniosynostoses;

MeSH definition : Premature closure of one or more CRANIAL SUTURES. It often results in plagiocephaly. Craniosynostoses that involve multiple sutures are sometimes associated with congenital syndromes such as ACROCEPHALOSYNDACTYLIA; and CRANIOFACIAL DYSOSTOSIS.;

MeSH synonym : craniosynostosis; plagiocephaly, synostotic; synostotic plagiocephaly; plagiocephaly, craniosynostosis; craniosynostosis plagiocephaly; craniostenosis; craniostenoses; Craniosynostose;

CISMeF synonym : anterior plagiocephalies, synostotic; brachycephalies; craniosynostosis plagiocephalies; plagiocephalies, craniosynostosis; plagiocephalies, synostotic; plagiocephalies, synostotic anterior; plagiocephalies, synostotic posterior; posterior plagiocephalies, synostotic; scaphocephalies; synostotic anterior plagiocephalies; synostotic plagiocephalies; synostotic posterior plagiocephalies; trigonocephalies; craniosynostosis, type 1;

DeCS synonym : Metopic Synostosis;

MeSH hyponym : synostotic posterior plagiocephaly; acrocephaly; trigonocephaly; brachycephaly; synostotic anterior plagiocephaly; scaphocephaly; Oxycephaly; Sagittal Synostosis; Sagittal Synostoses; Synostoses, Sagittal; Synostosis, Sagittal; Anterior Plagiocephaly, Synostotic; Plagiocephaly, Synostotic Anterior; Unilateral Coronal Synostosis; Coronal Synostoses, Unilateral; Coronal Synostosis, Unilateral; Synostoses, Unilateral Coronal; Synostosis, Unilateral Coronal; Unilateral Coronal Synostoses; Plagiocephaly, Synostotic Posterior; Posterior Plagiocephaly, Synostotic; Craniosynostosis, Lambdoidal; Craniosynostoses, Lambdoidal; Lambdoidal Craniosynostoses; Lambdoidal Craniosynostosis; Lambdoid Synostosis; Lambdoid Synostoses; Synostoses, Lambdoid; Synostosis, Lambdoid; Metopic Synostoses; Synostoses, Metopic; Synostosis, Metopic; 1 Craniosynostoses, Type; 1 Craniosynostosis, Type; Craniosynostoses, Type 1; Type 1 Craniosynostoses; Type 1 Craniosynostosis;

CISMeF hyponym : metopic synostosis;

Wikipedia link : https://en.wikipedia.org/wiki/Craniosynostosis;

Details

Origin ID

D003398;

UMLS CUI

C0010278;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Acrocephaly (disorder) [SNOMED CT concept]
- Brachycephaly [PASCAL descriptor]
- Brachycephaly [ACR pathology]
- Brachycephaly [HPO term]
- Brachycephaly [MedDRA Preferred Term]
- Interparietal craniosynostosis (disorder) [SNOMED CT concept]
- Isolated oxycephaly [ORDO Disease]
- Lambdoid synostosis [ICD-11 More detail]
- Metopic synostosis [HPO term]
- Oxycephaly [ICD-11 More detail]
- Oxycephaly [MedDRA Preferred Term]
- Oxycephaly [HPO term]
- Scaphocephaly [ICD-11 More detail]
- Scaphocephaly [HPO term]
- Trigonocephaly [PASCAL descriptor]
- Trigonocephaly [ICD-11 More detail]
- Trigonocephaly [HPO term]
- Trigonocephaly [HRDO Sign]
- acrocephaly [SNOMED Notion]
- brachycephaly [Radlex concept]
- brachycephaly [SNOMED Notion]
- craniofacial abnormalities [MedlinePlus Topic]
- msh homeobox 2 [HGNC gene]
- oxycephaly [Radlex concept]
- scaphocephaly [Radlex concept]
- trigonocephaly [SNOMED Notion]
- turricephaly [Radlex concept]
Currated CISMeF NLP mapping
- Craniostenosis [HPO term]
- Craniosynostosis [PASCAL descriptor]
- Craniosynostosis [ICD-10 Sub-category]
- Craniosynostosis [ICD-11 Subcategory]
- Craniosynostosis [ICD-10 Sub-category (who)]
- Craniosynostosis [HPO term]
- Craniosynostosis [MedDRA Preferred Term]
- Craniosynostosis [OMIM phenotypic series]
- Craniosynostosis [NCIt concept]
- Craniosynostosis [ACR pathology]
- Craniosynostosis [ORDO Disease]
- Craniosynostosis (coronal, sagittal, lambdoid sutures) [HPO term]
- Craniosynostosis syndrome (disorder) [SNOMED CT concept]
- Craniosynostosis, coronal and lambdoidal [HPO term]
- craniosynostosis [DO Concept]
- craniosynostosis [Disease (Nov.)]
- craniosynostosis [Radlex concept]
- craniosynostosis syndrome [SNOMED Notion]
- premature closure of cranial sutures [MedDRA Preferred Term]
DO Cross reference
- craniosynostosis [DO Concept]
False UMLS correspondences (reviewed by CISMeF team)
- Coronal craniosynostosis [HPO term]
- Craniosynostosis of coronal, lambdoid, and/or metopic sutures [HPO term]
- Craniosynostosis, coronal and lambdoidal [HPO term]
- Lambdoidal craniosynostosis [HPO term]
- Occasional craniosynostosis [HPO term]
- Orbital craniosynostosis [HPO term]
- Premature craniosynostosis [HPO term]
- Sagittal craniosynostosis [HPO term]
- Unilateral craniosynostosis [HPO term]
- premature closure of cranial sutures [MedDRA Preferred Term]
- primary coronal and lambdoid craniosynostosis [HPO term]
False automatic mappings
- Brachycephaly (disorder) [SNOMED CT concept]
- Dolichocephaly [HPO term]
- Scaphocephaly [MedDRA Preferred Term]
- Scaphycephaly (disorder) [Inactive SNOMED CT concept]
- Trigonocephaly (disorder) [SNOMED CT concept]
- scaphocephaly [SNOMED Notion]
HPO term
- Brachycephaly [HPO term]
- Craniosynostosis [HPO term]
- Lambdoidal craniosynostosis [HPO term]
- Metopic synostosis [HPO term]
- Oxycephaly [HPO term]
- Premature closure of fontanelles [HPO term]
- Scaphocephaly [HPO term]
- Trigonocephaly [HPO term]
- Turricephaly [HPO term]
Manual BTNT mappings - CISMeF
- Non-syndromic craniosynostosis [ORDO Disease]
- Syndromic craniosynostosis [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Craniosynostosis syndrome or cranial ossification disease [ORDO Disease]
- Genetic cranial malformation [ORDO Disease]
ORDO relation(s)
- Craniosynostosis [ORDO Disease]
Record concept(s)
- Craniosynostosis, Type 1 [MeSH concept]
- Metopic Synostosis [MeSH concept]
- acrocephaly [MeSH concept]
- brachycephaly [MeSH concept]
- craniosynostoses [MeSH concept]
- scaphocephaly [MeSH concept]
- synostotic anterior plagiocephaly [MeSH concept]
- synostotic posterior plagiocephaly [MeSH concept]
- trigonocephaly [MeSH concept]
Related MeSH Supplementary Concept(s)
- Craniosynostosis-Mental retardation syndrome of lin and gettig [MeSH Supplementary Concept]
- Fine-Lubinsky syndrome [MeSH Supplementary Concept]
- Hunter-McAlpine syndrome [MeSH Supplementary Concept]
- Jackson-Weiss syndrome [MeSH Supplementary Concept]
- aurocephalosyndactyly [MeSH Supplementary Concept]
- baraitser rodeck garner syndrome [MeSH Supplementary Concept]
- bohring syndrome [MeSH Supplementary Concept]
- calabro syndrome [MeSH Supplementary Concept]
- cole carpenter syndrome [MeSH Supplementary Concept]
- cranioectodermal dysplasia [MeSH Supplementary Concept]
- craniometaphyseal dysplasia, autosomal recessive type [MeSH Supplementary Concept]
- craniosynostosis mental retardation clefting syndrome [MeSH Supplementary Concept]
- craniosynostosis microcephaly with chromosomal breakage and other abnormalities [MeSH Supplementary Concept]
- craniosynostosis radial aplasia syndrome [MeSH Supplementary Concept]
- craniosynostosis syndrome, autosomal recessive [MeSH Supplementary Concept]
- craniosynostosis with anomalies of the cranial base and digits [MeSH Supplementary Concept]
- craniosynostosis with ectopia lentis [MeSH Supplementary Concept]
- craniosynostosis with fibular aplasia [MeSH Supplementary Concept]
- craniosynostosis with ocular abnormalities and hallucal defects [MeSH Supplementary Concept]
- craniosynostosis, adelaide type [MeSH Supplementary Concept]
- craniosynostosis, anal anomalies, and porokeratosis [MeSH Supplementary Concept]
- craniosynostosis, calcification of basal ganglia, and facial dysmorphism [MeSH Supplementary Concept]
- craniosynostosis, philadelphia type [MeSH Supplementary Concept]
- craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus [MeSH Supplementary Concept]
- craniosynostosis, type 2 [MeSH Supplementary Concept]
- craniotelencephalic dysplasia [MeSH Supplementary Concept]
- cutis gyrata syndrome of beare and stevenson [MeSH Supplementary Concept]
- furlong syndrome [MeSH Supplementary Concept]
- genoa syndrome [MeSH Supplementary Concept]
- hordnes engebretsen knudtson syndrome [MeSH Supplementary Concept]
- iida kannari syndrome [MeSH Supplementary Concept]
- kleeblattschaedel syndrome [MeSH Supplementary Concept]
- lowry maclean syndrome [MeSH Supplementary Concept]
- mehta lewis patton syndrome [MeSH Supplementary Concept]
- muenke syndrome [MeSH Supplementary Concept]
- oculopalatoskeletal syndrome [MeSH Supplementary Concept]
- opitz trigonocephaly syndrome [MeSH Supplementary Concept]
- pfeiffer tietze welte syndrome [MeSH Supplementary Concept]
- piepkorn karp hickok syndrome [MeSH Supplementary Concept]
- plagiocephaly and X-linked mental retardation [MeSH Supplementary Concept]
- polycystic kidney disease, potter type I, with microbrachycephaly, hypertelorism, and brachymelia [MeSH Supplementary Concept]
- scaphocephaly, maxillary retrusion, and mental retardation [MeSH Supplementary Concept]
- shprintzen golberg craniosynostosis [MeSH Supplementary Concept]
- skeletal dysplasia, san diego type [MeSH Supplementary Concept]
- spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation [MeSH Supplementary Concept]
- trigonobrachycephaly, bulbous bifid nose, micrognathia, and abnormalities of the hands and feet [MeSH Supplementary Concept]
- trigonocephaly, nonsyndromic [MeSH Supplementary Concept]
See also inter- (CISMeF)
- Brachycephaly [ICD-11 More detail]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Craniostenosis [HPO term]
- Craniosynostosis [MedDRA Preferred Term]
- Craniosynostosis [ORDO Disease]
- Craniosynostosis [ICD-10 Sub-category]
- Craniosynostosis [ACR pathology]
- Craniosynostosis [HPO term]
- Craniosynostosis [ICD-10 Sub-category (who)]
- Craniosynostosis [PASCAL descriptor]
- Craniosynostosis [NCIt concept]
- Craniosynostosis (coronal, sagittal, lambdoid sutures) [HPO term]
- Craniosynostosis 1 [OMIM Phenotype]
- Craniosynostosis syndrome (disorder) [SNOMED CT concept]
- Non-syndromic craniosynostosis [ORDO Disease]
- Premature closure of cranial sutures [MedDRA LLT]
- craniosynostosis [Radlex concept]
- craniosynostosis [DO Concept]
- craniosynostosis [Disease (Nov.)]
- craniosynostosis syndrome [SNOMED Notion]
Validated automatic mappings to BTNT
- Craniosynostosis 1 [OMIM Phenotype]
- Craniosynostosis 4 [OMIM Phenotype]
- Isolated plagiocephaly [ORDO Disease]
- Lambdoidal craniosynostosis [HPO term]
- Parieto-occipital craniosynostosis (disorder) [SNOMED CT concept]
- brachycephaly [Disease (Nov.)]
- trigonocephaly [Disease (Nov.)]

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