Disease #00041 (PCZ (PHEOCHROMOCYTOMA), OMIM:171300)
Official abbreviation |
PCZ |
Name |
PHEOCHROMOCYTOMA |
OMIM ID |
171300 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
SDHB |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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