An inherited susceptibility or predisposition to developing young-onset Parkinson disease, in which the cause of the disease is a mutation in the HTRA2 gene.
Comprehensive, easy-to-understand information about this condition
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microvascular complications of diabetes, susceptibility
MONDO:0000065
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MONDO:0000070
bacteremia, susceptibility
MONDO:0000108
pregnancy loss, recurrent, susceptibility
MONDO:0000144
autoimmune thyroid disease, susceptibility to
MONDO:0000162
susceptibility to HIV infection
MONDO:0004951