|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Huntington disease-like 2 (HDL2) is a severe neurodegenerative disorder considered part of the neuroacanthocytosis syndromes (see this term) characterized by a triad of movement, psychiatric, and cognitive abnormalities. (Orphanet Rare Disease Ontology, Orphanet_98934)|
|Downloads & Tools|
1 genes/proteins associated with the disease Huntington Disease-Like 2 from the curated CTD Gene-Disease Associations dataset.