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Huntington disease

1 OMIM reference -
1 associated gene
8 signs/symptoms

PROTEIN INTERACTIONS: 1

Familial short QT syndrome

3 OMIM references -
4 associated genes
No signs/symptoms info

Huntington disease

Familial short QT syndrome

HTT	(UniProt - OMIM)		CACNA2D1	(UniProt - OMIM)
			KCNH2	(UniProt - OMIM)
			KCNJ2	(UniProt - OMIM)
			KCNQ1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HTT	(0.63)	CACNA2D1

Citations in the biomedical literature:

Huntington disease		Familial short QT syndrome
	Synonym(s): - Huntington chorea		Synonym(s): - SQTS

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare cardiac disease - Rare genetic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: any age Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D006816		External references: 3 OMIM references - No MeSH references

Huntington disease
	Frequent - Abnormal cry / voice / phonation disorder / nasal speech - Autosomal dominant inheritance - Cortical atrophy without hydrocephaly / cerebral hemiatrophy / subcortical atrophy - EEG anomalies - Hypertonia / spasticity / rigidity / stiffness - Movement disorder - Psychic / behavioural troubles - Psychic / psychomotor regression / dementia / intellectual decline
Familial short QT syndrome
(no data available)