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Descriptor English: Hereditary Breast and Ovarian Cancer Syndrome
Descriptor Spanish: Síndrome de Cáncer de Mama y Ovario Hereditario
Descriptor síndrome hereditario de cáncer de mama y ovario
Entry term(s) síndrome de cáncer de mama y ovario hereditario
Scope note: SÍNDROME DE CÁNCER HEREDITARIO autosómico dominante en el cual una mutación con mayor frecuencia en BRCA1 o BRCA2, se asocia con un significativo incremento en el riesgo de cáncer de ovario o mama.
Descriptor Portuguese: Síndrome Hereditária de Câncer de Mama e Ovário
Descriptor French: Syndrome héréditaire de cancer du sein et de l'ovaire
Entry term(s): HBOC Syndrome
HBOC Syndromes
Syndrome, HBOC
Syndromes, HBOC
Tree number(s): C04.588.180.483
C04.588.322.455.431
C04.700.517
C12.050.351.500.056.630.705.431
C12.050.351.937.418.685.431
C12.100.250.056.630.705.431
C12.900.418.685.431
C16.320.700.517
C17.800.090.500.483
C19.344.410.431
C19.391.630.705.431
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D061325
Scope note: Autosomal dominant HEREDITARY CANCER SYNDROME in which a mutation most often in either BRCA1 or BRCA2 is associated with a significantly increased risk for breast and ovarian cancers.
Annotation: coordinate IM with histological type of neoplasm (IM) if pertinent
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
Previous Indexing: Breast Neoplasms (1984-2011)
Ovarian Neoplasms (1989-2011)
Public MeSH Note: 2012
History Note: 2012
Related: BRCA1 Protein MeSH
BRCA2 Protein MeSH
DeCS ID: 54480
Unique ID: D061325
NLM Classification: WP 870
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2012/01/01
Date of Entry: 2011/06/24
Revision Date: 2018/06/29
Hereditary Breast and Ovarian Cancer Syndrome - Preferred
Concept UI M0556977
Scope note Autosomal dominant HEREDITARY CANCER SYNDROME in which a mutation most often in either BRCA1 or BRCA2 is associated with a significantly increased risk for breast and ovarian cancers.
Preferred term Hereditary Breast and Ovarian Cancer Syndrome
Entry term(s) HBOC Syndrome
HBOC Syndromes
Syndrome, HBOC
Syndromes, HBOC



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