Huntington Disease-Like 2 Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:C564708
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Genes

1 genes/proteins associated with the disease Huntington Disease-Like 2 from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
JPH3 junctophilin 3 2.88009