Achondrogenesis

Preferred Label : Achondrogenesis;

NCIt definition : A rare group of disorders characterized by defective development of bones and cartilage.;

Details

Origin ID

C84527;

UMLS CUI

C0001079;

Automatic exact mappings (from CISMeF team)
- Achondrogenesis [OMIM phenotypic series]
Currated CISMeF NLP mapping
- Achondrogenesis [PASCAL descriptor]
- Achondrogenesis [ACR pathology]
- Achondrogenesis [ICD-10 Sub-category]
- Achondrogenesis [ICD-11 Sub-sub category]
- Achondrogenesis [ICD-10 Sub-category (who)]
- Achondrogenesis [ORDO Disease]
- Achondrogenesis [MedDRA LLT]
- Achondrogenesis (disorder) [SNOMED CT concept]
- achondrogenesis [MeSH concept]
- achondrogenesis [MeSH Supplementary Concept]
- achondrogenesis [DO Concept]
- achondrogenesis, nos [SNOMED Notion]
See also inter- (CISMeF)
- Hypochondrogenesis [ICD-11 Sub-sub category]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Achondrogenesis [ORDO Disease]
- Achondrogenesis [MedDRA LLT]
- Achondrogenesis [ICD-10 Sub-category]
- Achondrogenesis [PASCAL descriptor]
- Achondrogenesis [ACR pathology]
- Achondrogenesis [ICD-11 Sub-sub category]
- Achondrogenesis [ICD-10 Sub-category (who)]
- Achondrogenesis (disorder) [SNOMED CT concept]
- achondrogenesis [MeSH concept]
- achondrogenesis [MeSH Supplementary Concept]
- achondrogenesis [DO Concept]
- achondrogenesis, nos [SNOMED Notion]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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