osteogenesis imperfecta, levin type

Preferred Label : osteogenesis imperfecta, levin type;

MeSH synonym : osteogenesis imperfecta with unusual skeletal lesions; levin syndrome 2; gnathodiaphyseal sclerosis; gnathodiaphyseal dysplasia;

Details

Origin ID

C536039;

UMLS CUI

C1833736;

Automatic exact mappings (from CISMeF team)
- Gnathodiaphyseal dysplasia [ICD-11 More detail]
- gnathodiaphyseal dysplasia [DO Concept]
Currated CISMeF NLP mapping
- Gnathodiaphyseal dysplasia [OMIM Phenotype]
- Gnathodiaphyseal dysplasia [ORDO Disease]
- Gnathodiaphyseal dysplasia syndrome (disorder) [SNOMED CT concept]
- gnathodiaphyseal dysplasia [Disease (Nov.)]
DO Cross reference
- gnathodiaphyseal dysplasia [DO Concept]
MeSH term(s) associated for indexing
- osteogenesis imperfecta [MeSH Descriptor]
Record concept(s)
- Osteogenesis imperfecta, Levin type [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Gnathodiaphyseal dysplasia [OMIM Phenotype]
- Gnathodiaphyseal dysplasia [ORDO Disease]
- Gnathodiaphyseal dysplasia syndrome (disorder) [SNOMED CT concept]
- gnathodiaphyseal dysplasia [Disease (Nov.)]
- gnathodiaphyseal dysplasia [DO Concept]

Keyword's position in hierarchy(ies) :

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