Focal epithelial hyperplasia, oral

Preferred Label : Focal epithelial hyperplasia, oral;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Heck disease; Feh, oral;

Inheritance : Autosomal recessive;

Prefixed ID : 229045;

Details

Origin ID

229045;

UMLS CUI

C0206067;

Automatic exact mappings (from CISMeF team)
- Focal epithelial hyperplasia of oral mucous membranes [ICD-11 Subcategory]
- focal epithelial hyperplasia [DO Concept]
Currated CISMeF NLP mapping
- Focal epithelial hyperplasia of mouth (disorder) [SNOMED CT concept]
- Heck disease [Disease (Nov.)]
- Heck's disease [MedDRA LLT]
- focal epithelial hyperplasia [MeSH Descriptor]
- focal epithelial hyperplasia [MeSH concept]
- focal epithelial hyperplasia of mouth [SNOMED Notion]
DO Cross reference
- focal epithelial hyperplasia [DO Concept]
HPO term(s)
- Abnormality of the mouth [HPO term]
- Autosomal recessive inheritance [HPO term]
- Focal epithelial hyperplasia of oral mucosa [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Focal Epithelial Hyperplasia [NCIt concept]
- Focal epithelial hyperplasia [MedDRA Preferred Term]
- Focal epithelial hyperplasia (morphologic abnormality) [SNOMED CT concept]
- Focal epithelial hyperplasia of mouth (disorder) [SNOMED CT concept]
- Heck disease [Disease (Nov.)]
- Heck's disease [MedDRA LLT]
- focal epithelial hyperplasia [SNOMED Notion]
- focal epithelial hyperplasia [MeSH Descriptor]
- focal epithelial hyperplasia [MeSH concept]
- focal epithelial hyperplasia [DO Concept]
- focal epithelial hyperplasia of mouth [SNOMED Notion]

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