MeSH Browser

MeSH Heading: Carney Complex
Tree Number(s): C04.557.450.565.550.312; C04.588.894.309.500; C14.280.459.500; C16.131.077.229; C16.131.831.108
Unique ID: D056733
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D056733
Scope Note: Autosomal dominant syndrome characterized by cardiac and cutaneous MYXOMAS; LENTIGINOSIS (spotty pigmentation of the skin), and endocrinopathy and its associated endocrine tumors. The cardiac myxomas may lead to SUDDEN CARDIAC DEATH and other complications in Carney complex patients. The gene coding for the PRKAR1A protein is one of the causative genetic loci (type 1). A second locus is at chromosome 2p16 (type 2).
Entry Term(s): Carney Complex, Type 1; Carney Complex, Type 2; Carney Complex, Type I; Carney Complex, Type II; Carney Myxoma-Endocrine Complex; Carney Myxoma-Endocrine Complex, Type II; Carney Syndrome; LAMB - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome; LAMB Syndrome; Myxoma, Spotty Pigmentation, and Endocrine Overactivity; NAME Syndrome; Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome
NLM Classification #: WG 226
Public MeSH Note: 2010
History Note: 2010
Date Established: 2010/01/01
Date of Entry: 2009/07/06
Revision Date: 2013/07/08

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

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: M0528903
Scope Note: Autosomal dominant syndrome characterized by cardiac and cutaneous MYXOMAS; LENTIGINOSIS (spotty pigmentation of the skin), and endocrinopathy and its associated endocrine tumors. The cardiac myxomas may lead to SUDDEN CARDIAC DEATH and other complications in Carney complex patients. The gene coding for the PRKAR1A protein is one of the causative genetic loci (type 1). A second locus is at chromosome 2p16 (type 2).
Terms: Carney Complex Preferred Term
Term UI T734006
Date01/27/2009
LexicalTag EPO
ThesaurusID; Carney Syndrome
Term UI T746545
Date02/25/2009
LexicalTag EPO
ThesaurusID; LAMB Syndrome
Term UI T734009
Date01/27/2009
LexicalTag ACX
ThesaurusID; Myxoma, Spotty Pigmentation, and Endocrine Overactivity
Term UI T734007
Date01/27/2009
LexicalTag NON
ThesaurusID; Carney Myxoma-Endocrine Complex
Term UI T734011
Date01/27/2009
LexicalTag EPO
ThesaurusID; LAMB - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome
Term UI T843514
Date05/02/2013
LexicalTag ABX
ThesaurusID GHR (2014); Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome
Term UI T843515
Date05/02/2013
LexicalTag NON
ThesaurusID GHR (2014); NAME Syndrome
Term UI T734008
Date01/27/2009
LexicalTag ACX
ThesaurusID

Carney Complex MeSH Descriptor Data 2024