MeSH Browser

MeSH Heading: Neoplastic Syndromes, Hereditary
Tree Number(s): C04.700; C16.320.700
Unique ID: D009386
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D009386
Annotation: coordinate with specific hereditary organ/neoplasm term or specific hereditary histological type
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.
Entry Version: NEOPL SYNDROMES HEREDITARY
Entry Term(s): Cancer Syndromes, Hereditary; Hereditary Cancer Syndromes; Hereditary Neoplastic Syndromes
NLM Classification #: QZ 210
Public MeSH Note: 87
History Note: 87
Date Established: 1987/01/01
Date of Entry: 1986/06/23
Revision Date: 2018/06/29

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

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.
Terms: Neoplastic Syndromes, Hereditary Preferred Term
Term UI T028004
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1987); Hereditary Cancer Syndromes
Term UI T028001
Date06/23/1986
LexicalTag NON
ThesaurusID UNK (19XX); Cancer Syndromes, Hereditary
Term UI T028002
Date06/23/1986
LexicalTag NON
ThesaurusID UNK (19XX); Hereditary Neoplastic Syndromes
Term UI T028003
Date06/23/1986
LexicalTag NON
ThesaurusID UNK (19XX)

Neoplastic Syndromes, Hereditary MeSH Descriptor Data 2024