Ex: C0006933 C0007102 C0007203 C3175196    or

CUI: C0406810   Carney Complex 
Autosomal dominant syndrome characterized by cardiac and cutaneous MYXOMAS; LENTIGINOSIS (spotty pigmentation of the skin), and endocrinopathy and its associated endocrine tumors. The cardiac myxomas may lead to SUDDEN CARDIAC DEATH and other complications in Carney complex patients. The gene coding for the PRKAR1A protein is one of the causative genetic loci (type 1). A second locus is at chromosome 2p16 (type 2).

rdfs:seeAlso — C0000768 C0006111 C0015127 C0205269 C0231218 C1314792 C1331418 C1457887 C0012634 C0026538 C0178685 C0221423 C0231172 C0679215 C0683323 C0683324 C0683337 C0699749 C1514815 C2359469 C3540542 C0016689 C0036945 C1123019 C2314867 C0017342 C0017361 C0178491 C0178492 C0441748 C0443147 C0678942 C0683222 C0683223 C1527180 C3899988 C3899989 C0014130 C1332133 C0039082 C0567439 C0700114 C0596913 C0683003 C0683004 C0751282 C1704241 C0018792 C0078994 C0225832 C0225844 C0225860 C0524422 C0928075 C0031911 C0031916 C0682898 C1571592 C1844592 C0221912 C0444099 C0814995 C0206736 C0265985 C0334447 C0334448 C0346094 C1333268 C0221941 C0085666 C0235752 C0474967 C0027960 C0027962 C0206737 C0334082 C0334433 C0473583 C1318558 C1456781 C0027086 C0346066 C0751283 C1523872 C3158972 C0205413 C3542930 C0151241 C0518959 C0518960 C1850635 C0023321 C0149722 C0439703 C0019932 C0014133 C0014136 C0729511 C3159084

skos:closeMatch —

skos:exactMatch — C0406810

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