Disease #03634 (SPG46 (paraplegia, spastic, type 46, autosomal recessive (SPG-46)), OMIM:614409)

Official abbreviation SPG46
Name paraplegia, spastic, type 46, autosomal recessive (SPG-46)
OMIM ID 614409
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene GBA2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00054872 Pat15 PubMed: van de Warrenburg 2016, Journal: van de Warrenburg 2016 - M - - - - - - - SPG46 hereditary spastic paraplegia, ataxia, cataract, neuropathy, mild ID, thin corpus callosum, white matter changes GBA2 GBA2 1 1 Erik-Jan Kamsteeg
00299449 - family, 2 affected HSP46 F - Ethiopia African - - - - SPG46 Dementia Ataxia Dystonia GBA2 GBA2 2 2 Katja Kloth
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