Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hypomyelination with atrophy of basal ganglia and cerebellum
Primary dystonia, DYT4 type

TUBB4A TUBB4A


COMMON
GENES
TUBB4A



Citations in the biomedical literature:


Hypomyelination with atrophy of basal ganglia and cerebellum
TUBB4A
Primary dystonia, DYT4 type



Hypomyelination with atrophy of basal ganglia and cerebellum
Primary dystonia, DYT4 type

Synonym(s):
- H-ABC

Synonym(s):
- DYT4
- Hereditary whispering dysphonia

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

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.