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Descriptor English: Carney Complex
Descriptor Spanish: Complejo de Carney
Descriptor Portuguese: Complexo de Carney
Descriptor French: Complexe de Carney
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 Myxoma-Endocrine Complex
Carney Myxoma-Endocrine Complex, Type II
Carney Syndrome
Complex, Carney
Complex, Carney Myxoma-Endocrine
LAMB - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome
LAMB Syndrome
LAMB Syndromes
Myxoma, Spotty Pigmentation, and Endocrine Overactivity
Myxoma-Endocrine Complex, Carney
NAME Syndrome
NAME Syndromes
Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome
Syndrome, Carney
Syndrome, LAMB
Syndromes, LAMB
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
RDF Unique Identifier: https://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).
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
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: 2010
History Note: 2010
DeCS ID: 53487
Unique ID: D056733
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2010/01/01
Date of Entry: 2009/07/06
Revision Date: 2013/07/08
Carney Complex - Preferred
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).
Preferred term Carney Complex
Entry term(s) Carney Myxoma Endocrine Complex
Carney Myxoma-Endocrine Complex
Carney Syndrome
Complex, Carney
Complex, Carney Myxoma-Endocrine
LAMB - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome
LAMB Syndrome
LAMB Syndromes
Myxoma, Spotty Pigmentation, and Endocrine Overactivity
Myxoma-Endocrine Complex, Carney
NAME Syndrome
NAME Syndromes
Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome
Syndrome, Carney
Syndrome, LAMB
Syndromes, LAMB
Carney Complex, Type 1 - Narrower
Concept UI M0528904
Scope note Carney Complex, Type 1
Preferred term Carney Complex, Type 1
Entry term(s) Carney Complex, Type I
Carney Complex, Type 2 - Narrower
Concept UI M0528905
Preferred term Carney Complex, Type 2
Entry term(s) Carney Complex, Type II
Carney Myxoma Endocrine Complex, Type II
Carney Myxoma-Endocrine Complex, Type II



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