Hyperostosis Frontalis Interna

Preferred Label : Hyperostosis Frontalis Interna;

NCIt definition : A condition of unknown etiology characterized by thickening of the inner table of the frontal bone of the skull. It is seen more often in females and is usually bilateral.;

Details

Origin ID

C84772;

UMLS CUI

C0020494;

Automatic exact mappings (from CISMeF team)
- Internal frontal hyperostosis [PASCAL descriptor]
- Morgagni-Stewart-Morel syndrome [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Hyperostosis frontalis interna [HPO term]
- Hyperostosis frontalis interna [OMIM Phenotype]
- Hyperostosis interna frontalis (finding) [SNOMED CT concept]
- Morgagni-Stewart-Morel syndrome [ORDO Disease]
- hyperostosis frontalis interna [MeSH Descriptor]
- hyperostosis frontalis interna [MeSH concept]
- hyperostosis interna frontalis [SNOMED Notion]
Has associated anatomic sites
- Bone [NCIt concept]
- Connective and Soft Tissue [NCIt concept]
- Musculoskeletal System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hyperostosis frontalis interna [OMIM Phenotype]
- Hyperostosis frontalis interna [HPO term]
- Hyperostosis interna frontalis (finding) [SNOMED CT concept]
- Morgagni-Stewart-Morel syndrome [ORDO Disease]
- hyperostosis frontalis interna [MeSH concept]
- hyperostosis frontalis interna [MeSH Descriptor]
- hyperostosis interna frontalis [SNOMED Notion]
disease_has_normal_tissue_origin
- Connective and Soft Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Bone [NCIt concept]

Keyword's position in hierarchy(ies) :

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