Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
von Hippel-Lindau disease
OMIM:193300
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
05/24/2023
PubMed IDs:
10102622 10823831 12202531 15796386 18043261 1967104 1982450 2011596 20151405 21386872 2274658 22763871 2328994 24003980 25611110 28620007 2894613 29075773 31095066 31649892 7660122 8956040 9671762 9751722
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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