pheochromocytoma/paraganglioma syndrome 7
MONDO:0032771Mondo
Findings
No curated finding names pheochromocytoma/paraganglioma syndrome 7 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance · Typified by incomplete penetrance
- Onset and course
- Adult onset
HPO, annotations 2026-09-02
Features
2 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- ParagangliomaHPOHP:0002668
- 6 of 8 reported patients
- PheochromocytomaHPOHP:0002666
- 3 of 8 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- DLSTHGNC:2911
- Limited · Ambry Genetics · Autosomal dominant · 2023
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2020
Where it sits
Other names
1 name
Resolves to: pheochromocytoma/paraganglioma syndrome 7
- Also called
- paragangliomas 7