Parkinson disease 18, autosomal dominant, susceptibility to

Go to external page http://purl.obolibrary.org/obo/MONDO_0013653


Any hereditary late onset Parkinson disease in which the cause of the disease is a mutation in the EIF4G1 gene. [ MONDO:patterns/disease_series_by_gene ]

This is just here as a test because I lose it

Term information

Subsets

predisposition

abbreviation
PARK18 [ https://omim.org/entry/614251 MONDO:Lexical ]

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/specific_disease_by_dysfunctional_structure.yaml

definition

Any hereditary late onset Parkinson disease in which the cause of the disease is a mutation in the EIF4G1 gene.

exactMatch

http://identifiers.org/omim/614251

http://linkedlifedata.com/resource/umls/id/C3280271

has exact synonym

hereditary late onset Parkinson disease caused by mutation in EIF4G1

Parkinson disease 18, autosomal dominant, susceptibility to

EIF4G1 hereditary late onset Parkinson disease

has related synonym

susceptibility to autosomal dominant Parkinson disease 18

PARK18

id

MONDO:0013653