Disease #00730 (SYNS-1 (synostoses syndrome, multiple, type 1 (SYNS-1)), OMIM:186500)

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Official abbreviation	SYNS-1
Name	synostoses syndrome, multiple, type 1 (SYNS-1)
OMIM ID	186500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NOG
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A