Disease #01603 (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 0
Phenotype entries for this disease 0
Associated with 2 genes CCND1, VHL
Associated tissues -
Disease features -
Remarks -