Disease #01808 (GD3 (Gaucher disease, type III), OMIM:231000)

Official abbreviation GD3
Name Gaucher disease, type III
OMIM ID 231000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GBA
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-06-13 22:17:03 +02:00 (CEST)


Individuals

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00440097 MSM61 PubMed: Latham 1991 - - - United States white - - - - GD3 see paper; ..., oculomotor apraxia GBA GBA 2 1 Johan den Dunnen
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