Disease #03784 (SPG53 (paraplegia, spastic, type 53, autosomal recessive (SPG-53)), OMIM:614898)

Official abbreviation SPG53
Name paraplegia, spastic, type 53, autosomal recessive (SPG-53)
OMIM ID 614898
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 VPS37A
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

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00054873 Pat16 PubMed: van de Warrenburg 2016, Journal: van de Warrenburg 2016 - M - - - - - - - SPG53 SPG, ataxia, hypomimia FA2H FA2H 2 1 Erik-Jan Kamsteeg
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