Disease #03149 (SPG-42 (paraplegia, spastic, type 42, autosomal dominant (SPG-42)), OMIM:612539)

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Official abbreviation	SPG-42
Name	paraplegia, spastic, type 42, autosomal dominant (SPG-42)
OMIM ID	612539
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC33A1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A