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Huntington disease

1 OMIM reference -
1 associated gene
8 signs/symptoms

PROTEIN INTERACTIONS: 1

Acute myeloid leukemia with t(8;16)(p11;p13) translocation

2 associated genes
No signs/symptoms info

Huntington disease

Acute myeloid leukemia with t(8;16)(p11;p13) translocation

HTT	(UniProt - OMIM)		CREBBP	(UniProt - OMIM)
			KAT6A	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HTT	(0.87)	CREBBP

Citations in the biomedical literature:

Huntington disease		Acute myeloid leukemia with t(8;16)(p11;p13) translocation
	Synonym(s): - Huntington chorea		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare hematologic disease - Rare oncologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Neoplasms -

	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: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: D006816		External references: No 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
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
(no data available)