phenylketonurias

Preferred Label : phenylketonurias;

UMLS semantic type : T047 - Disease or Syndrome;

Détails

Origin ID

M0016567;

UMLS CUI

C0031485;

Automatic exact mappings (from CISMeF team)
- Other hyperphenylalaninaemias [ICD-10 Sub-category (who)]
- classical phenylketonuria [Artificial nutrition thesaurus concept]
- phenylketonuria [EMDN type]
Currated CISMeF NLP mapping
- Classical phenylketonuria (disorder) [SNOMED CT concept]
- PHENYLKETONURIA [WHO-ART Preferred Term]
- PKU [MedDRA LLT]
- Phenylalaninaemia [MedDRA LLT]
- Phenylalaninemia [MedDRA LLT]
- Phenylketonuria [PASCAL descriptor]
- Phenylketonuria [ICD-11 Subcategory]
- Phenylketonuria [MedDRA Preferred Term]
- Phenylketonuria [NCIt concept]
- Phenylketonuria [OMIM Phenotype]
- Phenylketonuria [ACR pathology]
- Phenylketonuria [ORDO Disease]
- Phenylketonuria (PKU) [MedDRA LLT]
- Phenylketonuria (disorder) [SNOMED CT concept]
- Phenylketonuria [PKU] [ICD-9 code]
- classical phenylketonuria [SNOMED Notion]
- phenylketonuria [Disease (Nov.)]
- phenylketonuria [DO Concept]
- phenylketonuria [MedlinePlus Topic]
MeSH narrower concept(s)
- hyperphenylalaninaemia [MeSH concept]
- phenylketonuria I [MeSH concept]
- phenylketonuria II [MeSH concept]
Related MeSH concept(s)
- hyperphenylalaninemia, Non-Phenylketonuric [MeSH concept]
Related record
- phenylketonurias [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- PHENYLKETONURIA [WHO-ART Preferred Term]
- PKU [MedDRA LLT]
- Phenylalaninaemia [MedDRA LLT]
- Phenylalaninemia [MedDRA LLT]
- Phenylketonuria [ORDO Disease]
- Phenylketonuria [ACR pathology]
- Phenylketonuria [MedDRA Preferred Term]
- Phenylketonuria [NCIt concept]
- Phenylketonuria (PKU) [MedDRA LLT]
- Phenylketonuria (disorder) [SNOMED CT concept]
- Phenylketonuria [PKU] [ICD-9 code]
- phenylketonuria [MedlinePlus Topic]
Validated automatic mappings to BTNT
- Classical Phenylketonuria [NCIt concept]

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