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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Autosomal dominant spastic paraplegia type 8
LMNA-related cardiocutaneous progeria syndrome

KIAA0196 LMNA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
KIAA0196
(0.63)
LMNA



Citations in the biomedical literature:


Autosomal dominant spastic paraplegia type 8
KIAA0196
LMNA-related cardiocutaneous progeria syndrome
LMNA



Autosomal dominant spastic paraplegia type 8
LMNA-related cardiocutaneous progeria syndrome

Synonym(s):
- SPG8

Synonym(s):
- LCPS

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

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

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: adulthood
Average age of death: adult
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C536867
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.