hawkinsinuria - CISMeF

Preferred Label : hawkinsinuria;

MeSH synonym : 4-Alpha-hydroxyphenylpyruvate hydroxylase deficiency;

Origin ID

C535845;

UMLS CUI

C2931042;

Automatic exact mappings (from CISMeF team)
- hawkinsinuria [DO Concept]
Currated CISMeF NLP mapping
- 4-Hydroxyphenylpyruvate dioxygenase deficiency (disorder) [SNOMED CT concept]
- 4-hydroxyphenylpyruvate dioxygenase deficiency [SNOMED Notion]
- Hawkinsinuria [ICD-11 More detail]
- Hawkinsinuria [OMIM Phenotype]
- Hawkinsinuria [ORDO Disease]
- Hawkinsinuria (disorder) [SNOMED CT concept]
DO Cross reference
- hawkinsinuria [DO Concept]
MeSH term(s) associated for indexing
- mixed function oxygenases [MeSH Descriptor]
- tyrosinemias [MeSH Descriptor]
ORDO relation(s)
- Hawkinsinuria [ORDO Disease]
Record concept(s)
- Hawkinsinuria [MeSH concept]
See also (suggested by CISMeF)
- 4-hydroxyphenylpyruvate dioxygenase [MeSH Descriptor]
- hawkinsin [MeSH Supplementary Concept]
See also inter- (CISMeF)
- Tyrosinaemia type 3 [ICD-11 More detail]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hawkinsinuria [ORDO Disease]
- Hawkinsinuria [OMIM Phenotype]
- Hawkinsinuria [ICD-11 More detail]
- Hawkinsinuria (disorder) [SNOMED CT concept]
- hawkinsinuria [DO Concept]