FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Carney complex ID (Ontology) DOID:0050471 (Human Disease)
Definition A syndrome characterized by myxomas, spotty pigmentation of the skin and endocrine overactivity.
Also Known As "Carney complex variant" ; "Carney Complex, Type 1" ; "Carney Complex, Type 2" (for all, see Synonyms field below)
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 Genes
 Carney complex       2
 for disease ribbon | Carney complex       2
 model of | Carney complex       2
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
disease                         |
 |__syndrome____________________|
                                Carney complex  2 rec.
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Is a autosomal dominant disease
syndrome
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Synonyms
  • "Carney complex variant" EXACT
    "Carney Complex, Type 1" EXACT
    "Carney Complex, Type 2" EXACT
    "Carney Syndrome" EXACT
    "LAMB Syndrome" EXACT
    "NAME Syndrome" EXACT
Secondary IDs
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GARD:1119
MESH:D056733
MIM:160980
MIM:605244
MIM:608837
NCI:C4705
ORDO:1359
SNOMEDCT_US_2023_03_01:733491005
UMLS_CUI:C0406810
UMLS_CUI:C1854540
UMLS_CUI:C2607929