osteogenesis imperfecta, type IX

Preferred Label : osteogenesis imperfecta, type IX;

CISMeF synonym : osteogenesis imperfecta, sillence type II/III, without abnormality of type I collagen; OI9;

MeSH synonym : OI, type IX; Osteogenesis Imperfecta, Sillence Type II-III, Without Abnormality of Type I Collagen; OI, type IX Osteogenesis Imperfecta, type IX; OI9 Osteogenesis Imperfecta 9; OI, type 9 Osteogenesis Imperfecta, type 9;

Details

Origin ID

C564921;

UMLS CUI

C1850169;

Automatic exact mappings (from CISMeF team)
- PPIB wt Allele [NCIt concept]
- osteogenesis imperfecta type 9 [DO Concept]
- peptidylprolyl isomerase B [ORDO Gene]
Currated CISMeF NLP mapping
- Osteogenesis imperfecta, type ix [OMIM Phenotype]
MeSH term(s) associated for indexing
- osteogenesis imperfecta [MeSH Descriptor]
Record concept(s)
- osteogenesis imperfecta, type IX [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Osteogenesis imperfecta, type ix [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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