| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/606438 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the huntington disease-like 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| JPH3 | junctophilin 3 |
