Disease #03536 (SPG47;CPSQ5 (spastic paraplegia, type 47 (SPG-47, palsy, cerebral, spastic quadriplegic, type 5)), OMIM:614066)

Official abbreviation SPG47;CPSQ5
Name spastic paraplegia, type 47 (SPG-47, palsy, cerebral, spastic quadriplegic, type 5)
OMIM ID 614066
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 1 gene AP4B1
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

2 entries on 1 page. Showing entries 1 - 2.
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00384652 - - - M likely Spain white - - - - SPG47;CPSQ5 - AP4B1, AP4E1, AP4M1, AP4S1, ATL1, BSCL2, REEP1, SPAST, SPG11, SPG20, SPG21 AP4B1 1 1 Clara Gómez
00442603 RDFA06 - two patients - yes Pakistan - - - - - SPG47;CPSQ5 - AP4B1 AP4B1 1 2 Sadaf Naz
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