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Disease association ontology term - MONDO:0017366 - hereditary pheochromocytoma-paraganglioma

Term summary

ID
MONDO:0017366
Name
hereditary pheochromocytoma-paraganglioma
Ontology or CV name
Disease association
Definition
Neoplasm predisposition characterized by an increased risk of paragangliomas (tumors that arise from neuroendocrine tissues distributed along the paravertebral axis from the base of the skull to the pelvis) and pheochromocytomas (paragangliomas that are confined to the adrenal medulla).

Parents

Annotation

Disease association

MONDO:0008192 - pheochromocytoma/paraganglioma syndrome 1

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MONDO:0011121 - pheochromocytoma/paraganglioma syndrome 2

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MONDO:0011544 - pheochromocytoma/paraganglioma syndrome 3

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MONDO:0007273 - pheochromocytoma/paraganglioma syndrome 4

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MONDO:0013602 - pheochromocytoma/paraganglioma syndrome 5

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MONDO:0032771 - pheochromocytoma/paraganglioma syndrome 7

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