loading...| Preferred Name |
hereditary pheochromocytoma-paraganglioma |
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| Synonyms |
familial pheochromocytoma-paraganglioma hereditary pheochromocytoma-paraganglioma hereditary paraganglioma-pheochromocytoma SDHx-related paraganglioma-pheochromocytoma |
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| Definitions |
Hereditary paraganglioma-pheochromocytomas (PGL/PCC) are rare neuroendocrine tumors represented by paragangliomas (occurring in any paraganglia from the skull base to the pelvic floor) and pheochromocytomas (adrenal medullary paragangliomas). |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0017366 |
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| has characteristic | ||
| has_exact_synonym |
familial pheochromocytoma-paraganglioma hereditary pheochromocytoma-paraganglioma |
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| has_related_synonym |
hereditary paraganglioma-pheochromocytoma SDHx-related paraganglioma-pheochromocytoma |
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| label |
hereditary pheochromocytoma-paraganglioma |
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| prefixIRI |
MONDO:0017366 |
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| prefLabel |
hereditary pheochromocytoma-paraganglioma |
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| seeAlso |
https://rarediseases.info.nih.gov/diseases/11984/hereditary-paraganglioma-pheochromocytoma |
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| textual definition |
Hereditary paraganglioma-pheochromocytomas (PGL/PCC) are rare neuroendocrine tumors represented by paragangliomas (occurring in any paraganglia from the skull base to the pelvic floor) and pheochromocytomas (adrenal medullary paragangliomas). |
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| subClassOf |