Disease #00214 (SPG12 (paraplegia, spastic, autosomal dominant, type 12 (SPG-12)), OMIM:604805)

Official abbreviation SPG12
Name paraplegia, spastic, autosomal dominant, type 12 (SPG-12)
OMIM ID 604805
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene RTN2
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

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00003012 Pat4mov;Pat11 PubMed: Neveling 2013, PubMed: van de Warrenburg 2016, Journal: van de Warrenburg 2016 - M - - - - - - - SPG12 hereditary spastic paraplegia RTN2 RTN2 1 1 Marcel Nelen
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