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Parkinson disease 13, autosomal dominant, susceptibility to

^ http://purl.obolibrary.org/obo/MONDO_0012466

Any young-onset Parkinson disease in which the cause of the disease is a mutation in the HTRA2 gene. [ MONDO:patterns/disease_series_by_gene ]

Term info

database cross reference
  • OMIM:610297 (MONDO:equivalentTo)
  • MESH:C565204 (MONDO:equivalentTo)
Subsets

predisposition

abbreviation
PARK13 [ OMIM:610297 MONDO:Lexical ]

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/4521

definition

Any young-onset Parkinson disease in which the cause of the disease is a mutation in the HTRA2 gene.

exactMatch

http://identifiers.org/mesh/C565204, https://omim.org/entry/610297

has exact synonym

Parkinson disease 13, autosomal dominant, susceptibility to, HTRA2 young-onset Parkinson disease, Parkinson disease 13, young-onset Parkinson disease caused by mutation in HTRA2

has related synonym

PARK13, susceptibility to autosomal dominant Parkinson disease 13

id

MONDO:0012466