neuroacanthocytosis, mcleod type

Preferred Label : neuroacanthocytosis, mcleod type;

MeSH note : mutation in XK gene;

MeSH synonym : McLeod syndrome;

Origin ID

C564038;

UMLS CUI

C0398568;

Automatic exact mappings (from CISMeF team)
- McLeod syndrome [ICD-11 More detail]
- X-linked Kx blood group antigen, Kell and VPS13A binding protein [ORDO Gene]
- X-linked Kx blood group antigen, Kell and VPS13A binding protein [HGNC gene]
CISMeF manual mappings
- McLeod neuroacanthocytosis syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- Blood group deletion syndrome (disorder) [SNOMED CT concept]
- McLeod neuroacanthocytosis syndrome [ICD-11 More detail]
- McLeod neuroacanthocytosis syndrome (disorder) [SNOMED CT concept]
- McLeod syndrome [Disease (Nov.)]
- McLeod syndrome [PASCAL descriptor]
- Mcleod syndrome [OMIM Phenotype]
MeSH term(s) associated for indexing
- neuroacanthocytosis [MeSH Descriptor]
Record concept(s)
- neuroacanthocytosis, mcleod type [MeSH concept]
See also inter- (CISMeF)
- McLeod phenotype (finding) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Blood group deletion syndrome (disorder) [SNOMED CT concept]
- McLeod neuroacanthocytosis syndrome [ORDO Disease]
- McLeod neuroacanthocytosis syndrome [ICD-11 More detail]
- McLeod syndrome [PASCAL descriptor]
- McLeod syndrome [Disease (Nov.)]
- McLeod syndrome [DO Concept]
- Mcleod syndrome [OMIM Phenotype]