karak syndrome

Preferred Label : karak syndrome;

Origin ID

C548029;

UMLS CUI

C2750220;

Automatic exact mappings (from CISMeF team)
- Infantile neuroaxonal dystrophy [ICD-11 More detail]
- Neurodegeneration with brain iron accumulation 2b [OMIM Phenotype]
Currated CISMeF NLP mapping
- Infantile Neuroaxonal Dystrophy [NCIt concept]
- Infantile neuroaxonal dystrophy [ORDO Disease]
- Infantile neuroaxonal dystrophy (disorder) [SNOMED CT concept]
- infantile neuroaxonal dystrophy [SNOMED Notion]
MeSH term(s) associated for indexing
- neuroaxonal dystrophies [MeSH Descriptor]
Record concept(s)
- Karak Syndrome [MeSH concept]
See also inter- (CISMeF)
- infantile neuroaxonal dystrophy [Disease (Nov.)]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]