worth syndrome

Preferred Label : worth syndrome;

MeSH synonym : osteosclerosis, autosomal dominant worth type with torus palatinus; hyperostosis corticalis generalisata congenita; benign hyperostosis corticalis generalisata; endosteal hyperostosis worth type; osteosclerosis, autosomal dominant; hyperostosis corticalis generalisata, benign form of worth, with torus palatinus; endosteal hyperostosis, autosomal dominant;

Details

Origin ID

C536748;

UMLS CUI

C0432273;

Automatic exact mappings (from CISMeF team)
- Endosteal hyperostosis, autosomal dominant [OMIM Phenotype]
- Worth disease (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Autosomal dominant osteosclerosis, Worth type [ICD-11 More detail]
- Endosteal hyperostosis, Worth type [ORDO Disease]
- Worth syndrome [DO Concept]
DO Cross reference
- Worth syndrome [DO Concept]
MeSH term(s) associated for indexing
- hyperostosis, cortical, congenital [MeSH Descriptor]
- osteopetrosis [MeSH Descriptor]
Record concept(s)
- Worth syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant osteosclerosis, Worth type [ICD-11 More detail]
- Endosteal hyperostosis, Worth type [ORDO Disease]
- Endosteal hyperostosis, autosomal dominant [OMIM Phenotype]
- Worth disease (disorder) [SNOMED CT concept]
- Worth syndrome [DO Concept]

Keyword's position in hierarchy(ies) :

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