Hallermann Syndrome

Preferred Label : Hallermann Syndrome;

NCIt synonyms : Hallermann's Syndrome; Hallermann-Streiff Syndrome;

NCIt definition : A very rare syndrome characterized by multiple congenital abnormalities including abnormally shaped head, mandibular hypoplasia, parrot nose, bilateral congenital cataracts, microphthalmia, dwarfism and hypotrichosis.;

Détails

Origin ID

C84746;

UMLS CUI

C0018522;

Automatic exact mappings (from CISMeF team)
- Hallermann Streiff François syndrome [PASCAL descriptor]
- Hallermann-Streiff-François syndrome [ICD-11 More detail]
Currated CISMeF NLP mapping
- Hallermann Streiff syndrome [Disease (Nov.)]
- Hallermann-Streiff syndrome [DO Concept]
- Hallermann-Streiff syndrome [ORDO Disease]
- Hallermann-Streiff syndrome (disorder) [SNOMED CT concept]
- Hallermann-streiff syndrome [OMIM Phenotype]
- hallermann's syndrome [MeSH Descriptor]
- hallermann's syndrome [MeSH concept]
- hallermann-streiff syndrome [SNOMED Notion]
DO Cross reference
- Hallermann-Streiff syndrome [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hallermann-Streiff syndrome [ORDO Disease]
- Hallermann-Streiff syndrome [DO Concept]
- Hallermann-Streiff syndrome (disorder) [SNOMED CT concept]
- Hallermann-streiff syndrome [OMIM Phenotype]
- hallermann's syndrome [MeSH concept]
- hallermann's syndrome [MeSH Descriptor]
- hallermann-streiff syndrome [SNOMED Notion]
disease_has_finding
- Rare Lesion [NCIt concept]

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

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