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 41 - 50 of 54 in total
HPO ID HPO Term
HP:0011760 Pituitary growth hormone cell adenoma
HP:0012041 Decreased fertility in males
HP:0012206 Abnormal sperm motility
HP:0012743 Abdominal obesity
HP:0012887 Ovarian serous cystadenoma
HP:0100008 Schwannoma
HP:0100013 Neoplasm of the breast
HP:0100618 Leydig cell neoplasia
HP:0100619 Sertoli cell neoplasm
HP:0100638 Neoplasm of the pharynx
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