has material basis in germline mutation in disease has feature VPS13A Chorea VPS13A-related neurodegenerative disease https://github.com/monarch-initiative/mondo/issues/9825 https://www.malacards.org/card/choreoacanthocytosis MONDO:0008695 Chac A form of neuroacanthocytosis and is characterized clinically by a Huntington disease-like phenotype with progressive neurological symptoms including movement disorders, psychiatric manifestations and cognitive disturbances, and caused by a variation in the VPS13A gene. Orphanet:2388 VPS13A disease CHAC ICD9:333.0 choreoacanthocytosis SCTID:66881004 DOID:0050766 NANDO:1200014 Levine-Critchley syndrome GARD:0003956 OMIM:200150 UMLS:C0393576 chorea-acanthocytosis MEDGEN:98277 neuroacanthocytosis epidermal disease hereditary peripheral neuropathy hereditary skin disorder