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1 OMIM reference -
1 associated gene
8 signs/symptoms
PROTEIN INTERACTIONS: 2
2 OMIM references -
14 associated genes
No signs/symptoms info
Huntington disease
Maternally-inherited Leigh syndrome

HTT MT-ATP6
MT-CO1
MT-CO2
MT-CO3
MT-ND1
MT-ND2
MT-ND3
MT-ND4
MT-ND5
MT-ND6
MT-TK
MT-TL1
MT-TV
MT-TW


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HTT
HTT
(0.68)
(0.68)
MT-CO2
MT-CO3



Citations in the biomedical literature:


Huntington disease
HTT
Maternally-inherited Leigh syndrome
MT-ATP6 MT-CO1 MT-CO2 MT-CO3 MT-ND1 MT-ND2
MT-ND3 MT-ND4 MT-ND5 MT-ND6 MT-TK MT-TL1
MT-TV MT-TW



Huntington disease
Maternally-inherited Leigh syndrome

Synonym(s):
- Huntington chorea

Synonym(s):
- MILS
- Maternally-inherited Leigh disease
- Maternally-inherited infantile subacute necrotizing encephalopathy

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare neurologic disease

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

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: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: mitochondrial inheritance

External references:
1 OMIM reference -
1 MeSH reference: D006816
External references:
2 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



Maternally-inherited Leigh syndrome

(no data available)