Disease #00041 (PCZ (PHEOCHROMOCYTOMA), OMIM:171300)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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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 2 genes	SDHB, VHL
Associated tissues	-
Disease features	-
Remarks	-
Date created	2017-05-15 10:49:02 +00:00 (UTC)
Date last edited	2023-06-16 10:05:48 +00:00 (UTC)