peroxisome biogenesis disorders

Preferred Label : peroxisome biogenesis disorders;

Origin ID

C536664;

UMLS CUI

C1832200;

Automatic exact mappings (from CISMeF team)
- Peroxisome biogenesis disorder [OMIM phenotypic series]
- Zellweger syndrome [DO Concept]
- disorders of peroxisomal biogenesis [Error of metabolism category]
CISMeF manual mappings
- Peroxisome Biogenesis Disorder [NCIt concept]
Currated CISMeF NLP mapping
- Disorders of peroxisome biogenesis [ICD-11 Subcategory]
- Peroxisome biogenesis disorder [ORDO Disease]
- Peroxisome biogenesis disorder (disorder) [SNOMED CT concept]
- peroxisomal biogenesis disorder [DO Concept]
MeSH term(s) associated for indexing
- peroxisomal disorders [MeSH Descriptor]
ORDO relation(s)
- Peroxisome biogenesis disorder [ORDO Disease]
Record concept(s)
- Peroxisome biogenesis disorders [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Disorders of peroxisome biogenesis [ICD-11 Subcategory]
- Peroxisome Biogenesis Disorder [NCIt concept]
- Peroxisome biogenesis disorder [ORDO Disease]
- Peroxisome biogenesis disorder (disorder) [SNOMED CT concept]
- peroxisomal biogenesis disorder [DO Concept]