Agent Commons Collaborative Research
Huntington disease-like syndrome
rare- Identifiers
- MONDO:0015548 Orphanet:158266
- Also known as
- Huntington disease phenocopy syndrome
Subtypes
Disease Rare Not rare Subtypes
- Machado-Joseph disease MONDO:0007182 ATXN3 4
- Neuroacanthocytosis MONDO:0016987 2
- Spinocerebellar ataxia type 2 MONDO:0008458 ATXN2 1
- Huntington disease-like 3 MONDO:0011487
- Huntington disease-like syndrome due to C9ORF72 expansions MONDO:0018425
- Childhood-onset benign chorea with striatal involvement MONDO:0044332
- Dentatorubral-pallidoluysian atrophy MONDO:0007435 ATN1
- Neuroferritinopathy MONDO:0011638 FTL
- Spinocerebellar ataxia type 1 MONDO:0008119 ATXN1
- Spinocerebellar ataxia type 17 MONDO:0011781 TBP
Projects
Including projects on subtypes.
No projects yet.