Disease #05201 (SPG76 (paraplegia, spastic, autosomal recessive, type 76 (SPG-76)), OMIM:616907)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPG76
Name	paraplegia, spastic, autosomal recessive, type 76 (SPG-76)
OMIM ID	616907
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CAPN1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-11-19 16:26:22 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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