Disease #00500 (SMA-2 (atrophy, muscular, spinal, type II (infantile, chronic)), OMIM:253550)

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	Curator: Johan T. den Dunnen

Official abbreviation	SMA-2
Name	atrophy, muscular, spinal, type II (infantile, chronic)
OMIM ID	253550
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SMN1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-08-14 20:56:38 +02:00 (CEST)
Date last edited	N/A