Carney complex

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Information
Disease name
Carney complex
Disease ID
DOID:0050471
Description
"A syndrome characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity." [url:http\://en.wikipedia.org/wiki/Carney_complex, url:http\://ghr.nlm.nih.gov/condition/carney-complex]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes Mutation Description Source Links
NCT ID Status Phase Summary Start date Completion date
NCT00001452 Completed Defining the Genetic Basis for the Development of Primary Pigmented Nodular Adrenocortical Disease (PPNAD) and the Carney Complex December 14, 1995
NCT01560260 Completed Phase 2 Linsitinib in Treating Patients With Gastrointestinal Stromal Tumors March 2012 October 2015
NCT03050268 Recruiting Familial Investigations of Childhood Cancer Predisposition April 6, 2017 March 31, 2037
Exact Synonym (Disease Ontology)
Carney complex variant
Exact Synonym (Disease Ontology)
Carney Complex, Type 1
Exact Synonym (Disease Ontology)
Carney Complex, Type 2
Exact Synonym (Disease Ontology)
Carney Syndrome
Exact Synonym (Disease Ontology)
LAMB Syndrome
Exact Synonym (Disease Ontology)
NAME Syndrome
Disase is a (Disease Ontology)
DOID:225
Cross Reference ID (Disease Ontology)
GARD:1119
Cross Reference ID (Disease Ontology)
MESH:D056733
Cross Reference ID (Disease Ontology)
MIM:160980
Cross Reference ID (Disease Ontology)
MIM:605244
Cross Reference ID (Disease Ontology)
MIM:608837
Cross Reference ID (Disease Ontology)
NCI:C4705
Cross Reference ID (Disease Ontology)
ORDO:1359
Cross Reference ID (Disease Ontology)
SNOMEDCT_US_2023_03_01:733491005
Cross Reference ID (Disease Ontology)
UMLS_CUI:C0406810
Cross Reference ID (Disease Ontology)
UMLS_CUI:C1854540
Cross Reference ID (Disease Ontology)
UMLS_CUI:C2607929
OrphaNumber from OrphaNet (Orphanet)
1359
MeSH unique ID (MeSH (Medical Subject Headings))
D056733