Bannayan-Riley-Ruvalcaba syndrome

Preferred Label : Bannayan-Riley-Ruvalcaba syndrome;

ICD-11 definition : Bannayan-Riley-Ruvalcaba syndrome is characterized by an abnormally large head (macrocephaly), multiple hamartomatous polyps in the intestines, benign tumors of fatty tissues just below the skin, and excessive growth before and after birth.;

Détails

Origin ID

357383447;

Automatic exact mappings (from CISMeF team)
- hamartoma syndrome, multiple [MeSH Descriptor]
Currated CISMeF NLP mapping
- Bannayan syndrome (disorder) [SNOMED CT concept]
- Bannayan-Riley-Ruvalcaba Syndrome [NCIt concept]
- Bannayan-Riley-Ruvalcaba Syndrome [MeSH concept]
- Bannayan-Riley-Ruvalcaba syndrome [PASCAL descriptor]
- Bannayan-Riley-Ruvalcaba syndrome [DO Concept]
- Bannayan-Riley-Ruvalcaba syndrome [ORDO Disease]
- Bannayan-Riley-Ruvalcaba syndrome [MedDRA Preferred Term]
- Bannayan-riley-ruvalcaba syndrome [OMIM Phenotype]
- Cowden syndrome 1 [OMIM Phenotype]
- Ruvalcaba Myhre Smith syndrome [Disease (Nov.)]
- Ruvalcaba-Myhre syndrome (disorder) [SNOMED CT concept]
- ruvalcaba-myhre syndrome [SNOMED Notion]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients