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 31 - 40 of 54 in total
HPO ID HPO Term
HP:0004944 Dilatation of the cerebral artery
HP:0005585 Spotty hyperpigmentation
HP:0006731 Follicular thyroid carcinoma
HP:0006753 Neoplasm of the stomach
HP:0007565 Multiple cafe-au-lait spots
HP:0010619 Fibroadenoma of the breast
HP:0010732 Nodular changes affecting the eyelids
HP:0010785 Gonadal neoplasm
HP:0010788 Testicular neoplasm
HP:0011672 Cardiac myxoma
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