Disease #03015 (SPG18 (paraplegia, spastic, type 18 (SPG-18)), OMIM:611225)

Official abbreviation SPG18
Name paraplegia, spastic, type 18 (SPG-18)
OMIM ID 611225
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 ERLIN2
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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00054875 Pat26 PubMed: van de Warrenburg 2016, Journal: van de Warrenburg 2016 - M - - - - - - - SPG18 pure hereditary spastic paraplegia OPA1 OPA1 1 1 Erik-Jan Kamsteeg
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