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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Autosomal dominant spastic paraplegia type 13
Distal myopathy with posterior leg and anterior hand involvement

HSPD1 FLNC


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HSPD1
(0.63)
FLNC



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 13
HSPD1
Distal myopathy with posterior leg and anterior hand involvement
FLNC



Autosomal dominant spastic paraplegia type 13
Distal myopathy with posterior leg and anterior hand involvement

Synonym(s):
- SPG13

Synonym(s):
- Distal ABD-filaminopathy

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- 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 / 1 000 000
Average age onset: -
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: no data available
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C537485
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.