Disease #00203 (VHLS (VON HIPPEL-LINDAU SYNDROME), OMIM:193300)

Official abbreviation VHLS
Name VON HIPPEL-LINDAU SYNDROME
OMIM ID 193300
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene VHL
Associated tissues -
Disease features -
Remarks -
Date created 2024-06-03 08:01:41 +00:00 (UTC)
Date last edited N/A

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