Disease #00451 (Gaucher, atypical (Gaucher disease, atypical), OMIM:610539)

Official abbreviation Gaucher, atypical
Name Gaucher disease, atypical
OMIM ID 610539
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PSAP
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Disease features -
Remarks -
Date created 2014-07-09 21:21:23 +02:00 (CEST)
Date last edited 2021-06-30 08:23:02 +02:00 (CEST)


Individuals

1 entry on 1 page. Showing entry 1.
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00334906 PME26 PubMed: Courage 2021, Journal: Courage 2021 - M yes Turkey - - - - - Gaucher, atypical Onset age 8 of myoclonus. Associated with ataxia, horizontal gaze palsy, mild splenomegaly and mild intellectual disability. Progressive course, death age 19. - GBA 1 1 Carolina Courage
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