Huntington disease

MONDO:0007739

Also known as: HD, Huntington chorea, Huntington disease, Huntington's Disease, Huntington's chorea

MONDO:: MONDO:0007739
Orphanet:: 399 ↗
OMIM:: 143100 ↗

Rare disease54 associated genes

Description

Huntington disease (HD) is a rare neurodegenerative disorder of the central nervous system characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia.

Associated genes

SLC18A2
SLC6A3
MSH3
TARDBP
CRMP1
DNM1L
CASP2
FAN1
DLG4
RAB11A

+44 more genes — install the extension to see the full list inline on any page.

External references

MONDO browser ↗
Open Targets ↗
Orphanet (rare disease) ↗
OMIM ↗