achondrogenesis, type ii

Preferred Label : achondrogenesis, type ii;

Details

Origin ID

D4-00A13;

UMLS CUI

C0220685;

Automatic exact mappings (from CISMeF team)
- Achondrogenesis [ICD-10 Sub-category (who)]
- Hypochondrogenesis [ORDO Disease]
- Hypochondrogenesis (disorder) [SNOMED CT concept]
- hypochondrogenesis [MeSH concept]
- hypochondrogenesis [MeSH Supplementary Concept]
CISMeF manual mappings
- Hypochondroplasia [ORDO Disease]
Currated CISMeF NLP mapping
- Achondrogenesis type 2 [ICD-11 More detail]
- Achondrogenesis type 2 [MeSH concept]
- Achondrogenesis type 2 [ORDO Disease]
- Achondrogenesis, type II [OMIM Phenotype]
- Achondrogenesis, type II (disorder) [Inactive SNOMED CT concept]
- Achondrogenesis, type II (disorder) [SNOMED CT concept]
- Achondroplasia [ICD-10 Sub-category]
- Achondroplasia [ICD-10 Sub-category (who)]
- Hypochondroplasia [PASCAL descriptor]
- Hypochondroplasia [MedDRA Preferred Term]
- Hypochondroplasia [OMIM Phenotype]
- Hypochondroplasia (disorder) [SNOMED CT concept]
- Type II Achondrogenesis [NCIt concept]
- achondrogenesis type 2 [MeSH Supplementary Concept]
- achondrogenesis type II [DO Concept]
- hypochondroplasia [MeSH concept]
- hypochondroplasia [MeSH Supplementary Concept]
ICD-10 exact mapping(s)
- Achondrogenesis [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Chondrodysplastic malformation syndrome [ORDO Disease]
- FGFR3-related chondrodysplasia [ORDO Disease]
- Type 2 collagen-related bone disorder [ORDO Disease]
Metaterm(s)
- pediatrics [CISMeF Metaterm]
See also inter- (CISMeF)
- Acromesomelic dysplasia 2a [OMIM Phenotype]
- Hypochondroplasia [ICD-11 Sub-sub category]
- Hypochondroplasia [NCIt concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Achondrogenesis type 2 [MeSH concept]
- Achondrogenesis type 2 [ORDO Disease]
- Achondrogenesis type 2 [ICD-11 More detail]
- Achondrogenesis, type II [OMIM Phenotype]
- Achondrogenesis, type II (disorder) [SNOMED CT concept]
- Type II Achondrogenesis [NCIt concept]
- achondrogenesis type 2 [MeSH Supplementary Concept]
- achondrogenesis type II [DO Concept]
Validated automatic mappings to NTBT
- Achondroplasia [ICD-11 Sub-sub category]

Keyword's position in hierarchy(ies) :

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