Disease #03414 (SPG51 (Spastic paraplegia 51, autosomal recessive), OMIM:613744)

Official abbreviation SPG51
Name Spastic paraplegia 51, autosomal recessive
OMIM ID 613744
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 AP4E1
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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00080818 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - SPG51 Spastic paraplegia 51 (OMIM:613744) AP4E1 AP4E1 1 1 Daniel Trujillano
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