acrodysostosis

Preferred Label : acrodysostosis;

Details

Origin ID

D4-00D15;

UMLS CUI

C0220659;

Automatic exact mappings (from CISMeF team)
- Acrodysostosis [OMIM phenotypic series]
Currated CISMeF NLP mapping
- Acrodysostosis [ICD-11 More detail]
- Acrodysostosis [MedDRA Preferred Term]
- Acrodysostosis [MeSH concept]
- Acrodysostosis [ORDO Disease]
- Acrodysostosis (disorder) [SNOMED CT concept]
- acrodysostosis [DO Concept]
- acrodysostosis [Disease (Nov.)]
- acrodysostosis [MeSH Supplementary Concept]
Has phenotype(s) (HPO)
- Brachymelic dwarfism [HPO term]
- Broad upturned nasal tip [HPO term]
- Low nasal bridge [HPO term]
- Short broad hands [HPO term]
ICD-10 exact mapping(s)
- Other specified osteochondrodysplasias [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Nager syndrome [ORDO Disease]
- X-linked mandibulofacial dysostosis [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Acromelic dysplasia [ORDO Disease]
- Chondrodysplastic malformation syndrome [ORDO Disease]
- Syndrome with limb malformations as a major feature [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
SNOMED CT concept
- Acrodysostosis (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Acrodysostosis [ORDO Disease]
- Acrodysostosis [MeSH concept]
- Acrodysostosis [MedDRA Preferred Term]
- Acrodysostosis (disorder) [SNOMED CT concept]
- Arkless-Graham syndrome [MedDRA LLT]
- Maroteaux-Malamut syndrome [MedDRA LLT]
- Peripheral dysostosis [OMIM Phenotype]
- Peripheral dysostosis [ORDO Disease]
- acrodysostosis [MeSH Supplementary Concept]
- acrodysostosis [Disease (Nov.)]
- acrodysostosis [DO Concept]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

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