Disease #03812 (SPG-49 (paraplegia, spastic, type 49, autosomal recessive (SPG-49)), OMIM:615031)

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Official abbreviation	SPG-49
Name	paraplegia, spastic, type 49, autosomal recessive (SPG-49)
OMIM ID	615031
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TECPR2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A