| Descriptor English: | Neoplastic Syndromes, Hereditary | ||||||
| Descriptor Spanish: |
Síndromes Neoplásicos Hereditarios
| ||||||
| Descriptor Portuguese: | Síndromes Neoplásicas Hereditárias | ||||||
| Descriptor French: | Syndromes néoplasiques héréditaires | ||||||
| Entry term(s): |
Cancer Syndrome, Hereditary Cancer Syndromes, Hereditary Hereditary Cancer Syndrome Hereditary Cancer Syndromes Hereditary Neoplastic Syndrome Hereditary Neoplastic Syndromes Neoplastic Syndrome, Hereditary Syndrome, Hereditary Cancer Syndrome, Hereditary Neoplastic Syndromes, Hereditary Cancer Syndromes, Hereditary Neoplastic |
||||||
| Tree number(s): |
C04.700 C16.320.700 |
||||||
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D009386 | ||||||
| Scope note: | The condition of a pattern of malignancies within a family, but not every individual's necessarily having the same neoplasm. Characteristically the tumor tends to occur at an earlier than average age, individuals may have more than one primary tumor, the tumors may be multicentric, usually more than 25 percent of the individuals in direct lineal descent from the proband are affected, and the cancer predisposition in these families behaves as an autosomal dominant trait with about 60 percent penetrance. |
||||||
| Annotation: | coordinate with specific hereditary organ/neoplasm term or specific hereditary histological type |
||||||
| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
||||||
| Public MeSH Note: | 87 |
||||||
| History Note: | 87 |
||||||
| Entry Version: | NEOPL SYNDROMES HEREDITARY |
||||||
| DeCS ID: | 19258 | ||||||
| Unique ID: | D009386 | ||||||
| NLM Classification: | QZ 210 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1987/01/01 | ||||||
| Date of Entry: | 1986/06/23 | ||||||
| Revision Date: | 2018/06/29 |
-
-
DISEASES
Neoplasms [C04]Neoplasms
|
|
Neoplastic Syndromes, Hereditary
- Preferred
| Concept UI |
M0014613 |
| Scope note | The condition of a pattern of malignancies within a family, but not every individual's necessarily having the same neoplasm. Characteristically the tumor tends to occur at an earlier than average age, individuals may have more than one primary tumor, the tumors may be multicentric, usually more than 25 percent of the individuals in direct lineal descent from the proband are affected, and the cancer predisposition in these families behaves as an autosomal dominant trait with about 60 percent penetrance. |
| Preferred term | Neoplastic Syndromes, Hereditary |
| Entry term(s) |
Cancer Syndrome, Hereditary Cancer Syndromes, Hereditary Hereditary Cancer Syndrome Hereditary Cancer Syndromes Hereditary Neoplastic Syndrome Hereditary Neoplastic Syndromes Neoplastic Syndrome, Hereditary Syndrome, Hereditary Cancer Syndrome, Hereditary Neoplastic Syndromes, Hereditary Cancer Syndromes, Hereditary Neoplastic |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
