has material basis in germline mutation in XK hemolytic anemia familial hemolytic anemia obsolete syndrome associated with dilated cardiomyopathy neuroacanthocytosis XK-related neurodegenerative disease https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/9825 https://rarediseases.info.nih.gov/diseases/10731/mcleod-neuroacanthocytosis-syndrome https://www.malacards.org/card/mcleod_syndrome McLeod syndrome OMIM:300842 MONDO:0018945 icd11.foundation:1749275115 McLeod neuroacanthocytosis syndrome MCLDS NANDO:1200015 Orphanet:59306 UMLS:C0398568 XK disease MEDGEN:140765 ICD9:289.89 A form of neuroacanthocytosis and is characterized clinically by a Huntington's disease-like phenotype with an involuntary hyperkinetic movement disorder, psychiatric manifestations and cognitive alterations, and biochemically by absence of the Kx antigen and by weak expression of the Kell antigens. SCTID:234411007 MLS GARD:0010731 DOID:0112107 X-linked McLeod syndrome MESH:C564038