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.
Synonyms: HDL2
This is just here as a test because I lose it
Term information
database cross reference
- ICD-10:G10 (NTBT (ORPHA code's Narrower Term maps to a Broader Term))
- OMIM:606438 (E (Exact mapping: the two concepts are equivalent))
- UMLS:C1847987 (E (Exact mapping: the two concepts are equivalent))
- ICD-10:G10 (Attributed (The ICD10 code is attributed by Orphanet))
Term relations
Subclass of:
- disease
- present_in some Worldwide and has_point_prevalence_range some <1 / 1 000 000
- present_in some Worldwide and has_cases/families_value value 50.0
- has_inheritance some autosomal dominant
- has_age_of_onset some adult
- part_of some Neuroacanthocytosis
Related from: