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choreatic disease - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

choreatic disease

MONDO:0001595

Also known as:benign familial choreaBHCchorea, benign hereditary

Overview

A neurological condition affecting the involuntary movements. It is characterized by brief, non-repetitive irregular muscle contractions. It is seen in patients with Huntington's disease.

Clinical Presentation

Built from Human Phenotype Ontology (HPO) phenotype annotations and GeneReviews clinical descriptions. Features represent findings documented across known cases — not an exhaustive list of possible symptoms.

Features include very common findings: Difficulty walking (gait disturbance) and Movement abnormalities (abnormality of movement).

Organ System	Phenotype Count	Example Features
Brain and nerves	2	Difficulty walking (gait disturbance), Movement abnormalities (abnormality of movement)

Explore clinical features

Prognosis

Phenotype severity distribution: 2 very common features.

Estimated prevalence: <1 in 1,000,000 (VERY_RARE).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for choreatic disease.

10 publications have been identified in PubMed for choreatic disease. Research spans Case Report / Case Series (50%), Basic Science / Preclinical (30%), and Review / Meta-Analysis (10%).

Research Type	Count	% of Total
Patient case studies	5	50%

Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 7:47 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:1429

GARD

Genetic and Rare Diseases Info Center

GARD:15152

Questions for Your Care Team

→Are there specialists or centers of excellence for this condition in my area?
→Is there a patient registry I should consider joining?

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choreatic disease

Overview

Clinical Presentation

Explore clinical features

Prognosis

Research Landscape

Medical References

External Resources

Orphanet

GARD

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team

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