Disease #00217 (SPG8 (paraplegia, spastic, autosomal dominant, type 8 (SPG-8)), OMIM:603563)

Official abbreviation SPG8
Name paraplegia, spastic, autosomal dominant, type 8 (SPG-8)
OMIM ID 603563
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene KIAA0196
Associated tissues -
Disease features -
Remarks -
Date created 2013-10-02 11:35:03 +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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00003017 Pat9mov;Pat18 PubMed: Neveling 2013, PubMed: van de Warrenburg 2016, Journal: van de Warrenburg 2016 - F - - - - - - - SPG8 hereditary spastic paraplegia KIAA0196 KIAA0196 1 1 Marcel Nelen
00363503 178673 - - F - Germany - - - - - SPG8 spastic paraparesis KIAA0196 KIAA0196 1 1 Andreas Laner
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