Cytoscape Web
Click node...

Huntington disease
1 OMIM reference -
1 associated gene
8 signs/symptoms
PROTEIN INTERACTIONS: 1
Melanoma of soft part
3 associated genes
No signs/symptoms info
Huntington disease
Melanoma of soft part

HTT
(UniProt - OMIM)
 ATF1
(UniProt - OMIM)
CREB1
(UniProt - OMIM)
EWSR1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HTT
(0.49)
CREB1


Citations in the biomedical literature:


Huntington disease
HTT
Melanoma of soft part
ATF1 CREB1 EWSR1



Huntington disease
Melanoma of soft part

Synonym(s):
- Huntington chorea
Synonym(s):
- Clear cell sarcoma of soft tissue
- Clear cell sarcoma of the tendons and aponeuroses
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare oncologic 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:
(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



Melanoma of soft part

(no data available)