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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
/
Paraganglioma
Pheochromocytoma/paraganglioma syndrome 6
rare
Identifiers
MONDO:0032767
OMIM:618464
Causal genes
SLC25A11
Part of
Hereditary pheochromocytoma-paraganglioma
Paraganglioma
Also known as
paragangliomas 6 · PGL6
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