hyperostosis corticalis deformans juvenilis

Preferred Label : hyperostosis corticalis deformans juvenilis;

MeSH synonym : osteoectasia, familial; hyperphosphatasemia, chronic congenital idiopathic; hyperphosphatasia, familial idiopathic; juvenile paget disease; chronic congenital idiopathic hyperphosphatasemia; osteoectasia with hyperphosphatasia; familial osteoectasia; hyperphosphatasemia with bone disease; idiopathic hyperphosphatasia; juvenile paget's disease; osteochalasia desmalis familiaris; familial idiopathic hyperphosphatasemia; Paget disease of bone 5, juvenile-onset;

Détails

Origin ID

C537701;

UMLS CUI

C0268414;

CISMeF manual mappings
- Juvenile Paget disease [ORDO Disease]
Currated CISMeF NLP mapping
- Hyperphosphatasemia with bone disease (disorder) [SNOMED CT concept]
- Juvenile Paget Disease [NCIt concept]
- Juvenile Paget disease [ICD-11 Subcategory]
- Juvenile Paget's disease [MedDRA Preferred Term]
- Paget disease juvenile type [TUV Concept]
- Paget disease of bone 5, juvenile-onset [OMIM Phenotype]
- hyperphosphatasemia with bone disease [SNOMED Notion]
MeSH term(s) associated for indexing
- osteitis deformans [MeSH Descriptor]
Record concept(s)
- Hyperostosis corticalis deformans juvenilis [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hyperphosphatasemia with bone disease (disorder) [SNOMED CT concept]
- Juvenile Paget Disease [NCIt concept]
- Juvenile Paget disease [ORDO Disease]
- Juvenile Paget's disease [MedDRA Preferred Term]
- Paget disease juvenile type [TUV Concept]
- Paget disease of bone 5, juvenile-onset [OMIM Phenotype]
- hyperphosphatasemia with bone disease [SNOMED Notion]

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