Pheochromocytoma (PCC)

Alias:
Pheochromocytoma, Susceptibility to
Pheochromocytoma, Malignant
Chromaffin Cell Neoplasm
Medullary Chromaffinoma
Medullary Paraganglioma
Chromaffin Cell Tumor
Pheochromoblastoma
Phaeochromocytoma
Pheochromocytomas
Pcc
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Pheochromocytoma, also known as chromaffin cell neoplasm, is related to hereditary paraganglioma-pheochromocytoma syndromes and multiple endocrine neoplasia, type iia, and has symptoms including abdominal pain, chest pain and fever. An important gene associated with Pheochromocytoma is MAX (MYC Associated Factor X), and among its related pathways/superpathways are Pyruvate metabolism and TCA cycle III (animals). The drugs Doxazosin and Phenoxybenzamine have been mentioned in the context of this disorder. Affiliated tissues include adrenal gland and thyroid, and related phenotypes are hyperhidrosis and proteinuria
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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2610
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Medical Symptom

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Gene & Mutation

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MGI
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References Literature

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