Disease #04430 (SPG-73 (paraplegia, spastic?, autosomal dominant, type 73 (SPG-73)), OMIM:616282)

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Official abbreviation	SPG-73
Name	paraplegia, spastic?, autosomal dominant, type 73 (SPG-73)
OMIM ID	616282
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CPT1C
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	N/A