Switch to
Predicate | Object |
---|---|
rdf:type | |
calbc:hasCorrelation | |
skos:definition |
NCI: An autosomal dominant hereditary syndrome caused by mutations in the SDHD, SDHC, SDHB, and SDHAF2 genes. It is characterized by the development of paragangliomas and pheochromocytomas.
|
skos:inScheme | |
skos-xl:prefLabel | |
skos-xl:altLabel |