Spastic paraplegia - Paget disease of bone |
Hereditary cerebral cavernous malformation |
|
INTERACTOME ASSOCIATIONS (click on a score value to see the evidence) |
VCP
| (0.63)
| PDCD10
|
|
Citations in the biomedical literature:
Spastic paraplegia - Paget disease of bone |
Hereditary cerebral cavernous malformation |
|
Synonym(s): (no synonyms)
| |
Synonym(s): - Familial brain cavernous angioma - Familial brain cavernous hemangioma - Familial cerebral cavernoma - Familial cerebral cavernous malformation - Hereditary brain cavernous angioma - Hereditary brain cavernous hemangioma - Hereditary cerebral cavernoma
|
|
|
Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease
| |
Classification (Orphanet): - Rare circulatory system disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease
|
|
|
Classification (ICD10): (no data available)
| |
Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -
|
|
|
Epidemiological data: Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
| |
Epidemiological data: Class of prevalence: 1-5 / 10 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
|
|
|
External references: No OMIM references No MeSH references | |
External references: 3 OMIM references - No MeSH references
|
|
|
|
No signs/symptoms info available.