Disease #00048 (ISSD (sialic acid storage disorder, infantile (ISSD)), OMIM:269920)

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	Curator: Johan T. den Dunnen

Official abbreviation	ISSD
Name	sialic acid storage disorder, infantile (ISSD)
OMIM ID	269920
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC17A5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2012-08-30 17:40:36 +02:00 (CEST)
Date last edited	N/A