Progeria-associated arthropathy |
Myoclonus-dystonia syndrome |
LMNA | DRD2 | |||
DYT15 | () | |||
SGCE | ||||
TOR1A |
INTERACTOME ASSOCIATIONS (click on a score value to see the evidence) |
LMNA | (0.75) | TOR1A | |
Citations in the biomedical literature:
Progeria-associated arthropathy |
Myoclonus-dystonia syndrome |
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Synonym(s): (no synonyms)
| Synonym(s): - Alcohol-responsive dystonia- DYT11 - Hereditary essential myoclonus - Myoclonic dystonia | ||
Classification (Orphanet): - Rare genetic disease - Rare systemic or rheumatologic disease | Classification (Orphanet): - Rare genetic disease - Rare neurologic disease | ||
Classification (ICD10): (no data available)
| Classification (ICD10): - Diseases of the nervous system -
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Epidemiological data: (no data available)
| Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant | ||
External references: No OMIM references No MeSH references | External references: 1 OMIM reference - 1 MeSH reference: C536096 | ||