Acromesomelic dysplasias

ICD-11 code : LD24.9;

Preferred Label : Acromesomelic dysplasias;

ICD-11 definition : A group of rare disorders characterised by shortening of the bones of the forearms, lower legs, hands and feet.;

Details

Origin ID

2002361676;

UMLS CUI

C2930970;

Automatic exact mappings (from CISMeF team)
- Acromesomelic dysplasia [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Acromesomelic dysplasia [MeSH concept]
- Acromesomelic dysplasia [ORDO Disease]
- Acromesomelic dysplasia [OMIM phenotypic series]
- Acromesomelic dysplasia (disorder) [Inactive SNOMED CT concept]
- Acromesomelic dysplasia group (disorder) [SNOMED CT concept]
- acromesomelic dysplasia [DO Concept]
- acromesomelic dysplasia [MeSH Supplementary Concept]
- acromesomelic dysplasia syndrome [SNOMED Notion]
ICD-10 Mapping
- Other congenital malformations of musculoskeletal system [ICD-10 Sub-category]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Acromesomelic dysplasia [MeSH concept]
- Acromesomelic dysplasia 2c [OMIM Phenotype]
- Acromesomelic dysplasia Hunter-Thompson type (disorder) [SNOMED CT concept]
- Acromesomelic dysplasia group (disorder) [SNOMED CT concept]
- Acromesomelic dysplasia, Hunter-Thompson type [ORDO Disease]
- acromesomelic dysplasia [DO Concept]
- acromesomelic dysplasia [MeSH Supplementary Concept]
- acromesomelic dysplasia, Hunter-Thompson type [DO Concept]
Validated automatic mappings to BTNT
- Acromesomelic dysplasia 2c [OMIM Phenotype]
Validated automatic mappings to NTBT
- Congenital anomaly of musculoskeletal system (disorder) [SNOMED CT concept]
- Other congenital malformations of musculoskeletal system [ICD-10 Sub-category]

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