Huntington disease-like 2
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
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Summary
Huntington disease-like 2 is a rare disease[1]. It is known by 6 alternative names across languages and contexts.[2]
Key Facts
- Huntington disease-like 2's instance of is recorded as rare disease[3].
- Huntington disease-like 2's instance of is recorded as class of disease[4].
- Huntington disease-like 2 is a type of neurodegeneration[5].
- Huntington disease-like 2 is a type of Huntington's disease-like syndrome[6].
- Huntington disease-like 2 is a type of neuroacanthocytosis[7].
- Huntington disease-like 2's health specialty is recorded as neurology[8].
- Huntington disease-like 2's genetic association is recorded as JPH3[9].
- Huntington disease-like 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090104[10].
- Huntington disease-like 2's exact match is recorded as http://identifiers.org/doid/DOID:0090104[11].
- Huntington disease-like 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
Huntington disease-like 2 is known by 6 alternative names across languages and contexts.[2]