hyperlysinemia due to defect in lysine transport into mitochondria

Preferred Label : hyperlysinemia due to defect in lysine transport into mitochondria;

Origin ID

C565499;

UMLS CUI

C1855927;

Currated CISMeF NLP mapping
- Hyperlysinemia due to defect in lysine transport into mitochondria [OMIM Phenotype]
MeSH term(s) associated for indexing
- hyperlysinemias [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
Record concept(s)
- hyperlysinemia due to defect in lysine transport into mitochondria [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hyperlysinemia due to defect in lysine transport into mitochondria [OMIM Phenotype]