Huntington disease-like 2

Orpha code: 98934OMIM code: 606438

Definition

A rare severe neurodegenerative disorder that is considered one of the phenocopies of Huntington Disease (HD) affecting patients of African descent and characterized by a triad of movement (chorea, oculomotor, parkinsonism), psychiatric (prominently sadness, irritability and anxiety), and cognitive abnormalities (early cognitive decline and subcortical-like dementia).

Disease data
Classification

Disease

Synonyms
HDL2
HDL2
ORPHA code
98934
OMIM code
606438
ICD10 code
G10
ICD11 code
-

No additional description.

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