Disease #05069 (SOS (Spondyloocular syndrome (SOS)), OMIM:605822)

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Official abbreviation	SOS
Name	Spondyloocular syndrome (SOS)
OMIM ID	605822
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	XYLT2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 11:00:40 +02:00 (CEST)
Date last edited	N/A