hanhart syndrome - CISMeF

CISMeF

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Hanhart syndromeMeSH Supplementary Concept

Preferred Label : hanhart syndrome;

MeSH synonym : oromandibular limb hypogenesis complex;

Details

Origin ID

C535629;

UMLS CUI

C0595985;

Automatic exact mappings (from CISMeF team)
- Aglossia-adactyly syndrome (disorder) [SNOMED CT concept]
- Hypoglossia - hypodactyly [ICD-11 More detail]
Currated CISMeF NLP mapping
- Hanhart syndrome [PASCAL descriptor]
- Hanhart's syndrome (disorder) [SNOMED CT concept]
- Hypoglossia-hypodactylia [OMIM Phenotype]
- Hypoglossia-hypodactyly syndrome [ORDO Disease]
- hanhart's syndrome [SNOMED Notion]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- craniofacial abnormalities [MeSH Descriptor]
- limb deformities, congenital [MeSH Descriptor]
Record concept(s)
- Hanhart syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Aglossia-adactyly syndrome (disorder) [SNOMED CT concept]
- Hanhart syndrome [PASCAL descriptor]
- Hanhart's syndrome (disorder) [SNOMED CT concept]
- hanhart's syndrome [SNOMED Notion]

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24/05/2025

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