Disease #02078 (SPG5A (paraplegia, spastic, autosomal recessive, type 5A (SPG-5A)), OMIM:270800)

Official abbreviation SPG5A
Name paraplegia, spastic, autosomal recessive, type 5A (SPG-5A)
OMIM ID 270800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene CYP7B1
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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00039358 - - - - - Greece - - - - - SPG5A - CYP7B1 CYP7B1 2 1 David Lynch
00039359 - - - - - Greece - - - - - SPG5A - CYP7B1 CYP7B1 1 1 David Lynch
00046994 - - - - - - - - - - - SPG5A - CYP7B1 CYP7B1 1 1 David Lynch
00046995 - - - - - - - - - - - SPG5A - CYP7B1 CYP7B1 1 1 David Lynch
00403911 - - - F - Egypt - - - - - SPG5A Mental Retardation Progressive spastic paraparesis CYP7B1 CYP7B1 1 3 Sherifa Ahmed Hamed
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