facial asymmetry

Preferred Label : facial asymmetry;

MeSH definition : Congenital or acquired asymmetry of the face.;

MeSH synonym : asymmetry, facial; asymmetries, facial; facial asymmetries;

MeSH annotation : if congen use /congen; do not confuse with FACIAL HEMIATROPHY; since asymmetry is lateral, long face syndrome does not go here: index under FACIAL BONES /abnorm (IM) MALOCCLUSION or specific type (IM) SYNDROME (NIM);

Details

Origin ID

D005146;

UMLS CUI

C1306710;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [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)
- Craniofacial microsomia [OMIM Phenotype]
- Facial asymmetry [ICD-11 Category]
- Hemifacial microsomia [PASCAL descriptor]
- Hemifacial microsomia [ICD-11 More detail]
- Hemifacial microsomia (disorder) [SNOMED CT concept]
- Otomandibular syndrome [ORDO Disease]
- facio-auriculo-vertebral spectrum [SNOMED Notion]
Currated CISMeF NLP mapping
- Congenital facial asymmetry [ICD-10 Sub-category]
- Facial Asymmetry [NCIt concept]
- Facial asymmetry [ICD-10 Sub-category (who)]
- Facial asymmetry [HPO term]
- Facial asymmetry [MedDRA Preferred Term]
- Facial asymmetry (disorder) [SNOMED CT concept]
- asymmetry of face [SNOMED Notion]
- facial asymmetry [Disease (Nov.)]
False automatic mappings
- Hemifacial hyperplasia [OMIM Phenotype]
HPO term
- Facial asymmetry [HPO term]
Manual NTBT mappings (CISMeF)
- Oculo-auriculo-vertebral spectrum [ORDO Disease]
Mapping VCM hiérarchique
- deformity [VCM modifier]
Ne pas confondre avec
- facial hemiatrophy [MeSH Descriptor]
Record concept(s)
- facial asymmetry [MeSH concept]
Related MeSH Supplementary Concept(s)
- facial hemihypertrophy [MeSH Supplementary Concept]
- facial palsy, congenital, unilateral or bilateral [MeSH Supplementary Concept]
- fronto-facio-nasal dysplasia [MeSH Supplementary Concept]
- hemifacial hyperplasia with strabismus [MeSH Supplementary Concept]
- hemifacial myohyperplasia [MeSH Supplementary Concept]
- mehes syndrome [MeSH Supplementary Concept]
- oculodentoosseous dysplasia recessive [MeSH Supplementary Concept]
- opitz reynolds fitzgerald syndrome [MeSH Supplementary Concept]
See also
- facies [MeSH Descriptor]
See also (suggested by CISMeF)
- face [MeSH Descriptor]
See also inter- (CISMeF)
- Craniofacial microsomia [OMIM Phenotype]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Facial Asymmetry [NCIt concept]
- Facial asymmetry [MedDRA Preferred Term]
- Facial asymmetry [HPO term]
- Facial asymmetry (disorder) [SNOMED CT concept]
- asymmetry of face [SNOMED Notion]
- facial asymmetry [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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