atelosteogenesis, type 1

Preferred Label : atelosteogenesis, type 1;

MeSH synonym : spondylohumerofemoral hypoplasia; giant cell chondrodysplasia; atelosteogenesis, type I; atelosteogenesis type I; atelosteogenesis type 1;

Details

Origin ID

C535396;

UMLS CUI

C0265283;

CISMeF manual mappings
- Atelosteogenesis type I [ORDO Disease]
Currated CISMeF NLP mapping
- Atelosteogenesis (disorder) [SNOMED CT concept]
- Atelosteogenesis type 1 (disorder) [SNOMED CT concept]
- Atelosteogenesis type I [ICD-11 More detail]
- Atelosteogenesis, type I [OMIM Phenotype]
- atelosteogenesis [SNOMED Notion]
- atelosteogenesis type 1 [Disease (Nov.)]
MeSH term(s) associated for indexing
- osteochondrodysplasias [MeSH Descriptor]
ORDO relation(s)
- Atelosteogenesis type I [ORDO Disease]
Record concept(s)
- Atelosteogenesis, type 1 [MeSH concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Atelosteogenesis (disorder) [SNOMED CT concept]
- Atelosteogenesis type 1 (disorder) [SNOMED CT concept]
- Atelosteogenesis type I [ORDO Disease]
- Atelosteogenesis, type I [OMIM Phenotype]
- atelosteogenesis [SNOMED Notion]
- atelosteogenesis [DO Concept]
- atelosteogenesis [Disease (Nov.)]
- atelosteogenesis type 1 [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients