Carney complex

Summary
Synonym
  • Carney Complex, Type 1
  • Carney Complex, Type 2
  • Carney Syndrome
  • Carney complex variant
  • LAMB Syndrome
  • NAME Syndrome
Definition
A syndrome characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity.
Super Class
autosomal dominant disease syndrome
Disease Ontology
DOID:0050471
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5573 PRKAR1A protein kinase cAMP-dependent type I regulatory subunit alpha
The Human Phenotype Ontology
Displaying entries 21 - 30 of 54 in total
HPO ID HPO Term
HP:0001402 Hepatocellular carcinoma
HP:0001507 Growth abnormality
HP:0001580 Pigmented micronodular adrenocortical disease
HP:0001635 Congestive heart failure
HP:0001907 Thromboembolism
HP:0002890 Thyroid carcinoma
HP:0002894 Neoplasm of the pancreas
HP:0002895 Papillary thyroid carcinoma
HP:0003118 Increased circulating cortisol level
HP:0004324 Increased body weight
Displaying 1 entry
Gene ID Gene Symbol Description
50940 PDE11A phosphodiesterase 11A

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024