Maxillonasal dysplasia

Preferred Label : Maxillonasal dysplasia;

ICD-11 definition : Binder syndrome is a rare developmental anomaly, affecting primarily the anterior part of the maxilla and nasal complex. Affected individuals typically have an unusually flat, underdeveloped midface (midfacial hypoplasia), with an abnormally short nose and flat nasal bridge, underdeveloped upper jaw, relatively protruding lower jaw and/or a 'reverse overbite'' (or class III malocclusion).;

Détails

Origin ID

1099755052;

UMLS CUI

C0220692;

Currated CISMeF NLP mapping
- Maxillonasal dysplasia [ORDO Disease]
- Maxillonasal dysplasia [PASCAL descriptor]
- Maxillonasal dysplasia [MedDRA Preferred Term]
- Maxillonasal dysplasia syndrome (disorder) [SNOMED CT concept]
- Maxillonasal dysplasia, Binder type [MeSH concept]
- Maxillonasal dysplasia, binder type [OMIM Phenotype]
- maxillonasal dysplasia, binder type [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Binder syndrome [DO Concept]
- Binder's syndrome [MedDRA LLT]
- Maxillonasal dysplasia [MedDRA Preferred Term]
- Maxillonasal dysplasia [ORDO Disease]
- Maxillonasal dysplasia [PASCAL descriptor]
- Maxillonasal dysplasia syndrome (disorder) [SNOMED CT concept]
- Maxillonasal dysplasia, Binder type [MeSH concept]
- Maxillonasal dysplasia, binder type [OMIM Phenotype]
- maxillonasal dysplasia, binder type [MeSH Supplementary Concept]

Position du mot-clé dans l'(les) arborescence(s) :

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