donohue syndrome

Preferred Label : donohue syndrome;

UMLS semantic type : T019 - Congenital Abnormality; T047 - Disease or Syndrome;

Origin ID

M0528899;

UMLS CUI

C0265344;

Automatic exact mappings (from CISMeF team)
- Donohue syndrome [MedDRA Preferred Term]
- Leprechaunism [ICD-11 More detail]
- Leprechaunism [MedDRA LLT]
- Other specified endocrine disorders [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Donohue Syndrome [NCIt concept]
- Donohue syndrome [DO Concept]
- Donohue syndrome [OMIM Phenotype]
- Leprechaunism [PASCAL descriptor]
- Leprechaunism [ORDO Disease]
- Leprechaunism syndrome (disorder) [SNOMED CT concept]
- donohue syndrome [Disease (Nov.)]
- leprechaunism syndrome [SNOMED Notion]
Has phenotype(s) (HPO)
- Full lips [HPO term]
- Prenatal growth deficiency [HPO term]
- Prominent eyes [HPO term]
- patches [HPO term]
Related MeSH concept(s)
- Rabson-Mendenhall syndrome [MeSH concept]
Related record
- donohue syndrome [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Donohue Syndrome [NCIt concept]
- Donohue syndrome [OMIM Phenotype]
- Donohue syndrome [DO Concept]
- Donohue syndrome [MedDRA Preferred Term]
- Leprechaunism [ORDO Disease]
- Leprechaunism [PASCAL descriptor]
- Leprechaunism [MedDRA LLT]
- Leprechaunism syndrome (disorder) [SNOMED CT concept]
- donohue syndrome [Disease (Nov.)]
- leprechaunism syndrome [SNOMED Notion]