Disease #02642 (SPG7 (paraplegia, spastic, autosomal recessive, type 7 (SPG-7)), OMIM:607259)

Official abbreviation SPG7
Name paraplegia, spastic, autosomal recessive, type 7 (SPG-7)
OMIM ID 607259
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 4
Associated with 1 gene SPG7
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

5 entries on 1 page. Showing entries 1 - 5.
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00054863 Pat1 PubMed: van de Warrenburg 2016, Journal: van de Warrenburg 2016 - F no Netherlands - - - - - SPG7 pure ataxia only SPG7 SPG7 2 1 Erik-Jan Kamsteeg
00054864 Pat2 PubMed: van de Warrenburg 2016, Journal: van de Warrenburg 2016 - M - - - - - - - SPG7 pure ataxia only SPG7 SPG7 2 1 Erik-Jan Kamsteeg
00054865 Pat3 PubMed: van de Warrenburg 2016, Journal: van de Warrenburg 2016 - M - - - - - - - SPG7 HSP and ataxia, mild pyramidal signs lower limbs SPG7 SPG7 2 1 Erik-Jan Kamsteeg
00152016 - - - - - - - - - - - SPG7 - CYP7B1, MARS2, SPG7 SPG7 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00403898 - - - M yes Egypt - - - - - SPG7 cerebellar ataxia Spastic lower limbs, hyperreflexia, intact abdominal reflexes peripheral neuropathy pes cavus SPG7 SPG7 1 1 Sherifa Ahmed Hamed
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