Familial rhabdoid tumor |
Hereditary persistence of fetal hemoglobin - sickle cell disease |
Citations in the biomedical literature:
Familial rhabdoid tumor |
Hereditary persistence of fetal hemoglobin - sickle cell disease |
|
Synonym(s): - RTPS - Rhabdoid tumor predisposition syndrome
| |
Synonym(s): - HPFH - sickle cell disease
|
|
|
Classification (Orphanet): - Rare genetic disease - Rare oncologic disease
| |
Classification (Orphanet): - Rare genetic disease - Rare hematologic disease
|
|
|
Classification (ICD10): (no data available)
| |
Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
|
|
|
Epidemiological data: Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
| |
Epidemiological data: Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
|
|
|
External references: 2 OMIM references -
No MeSH references | |
External references: No OMIM references No MeSH references
|
|
|
|
No signs/symptoms info available.