Disease #00180 (RRS (Robinow syndrome, autosomal recessive (RRS)), OMIM:268310)

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	Curator: Johan T. den Dunnen

Official abbreviation	RRS
Name	Robinow syndrome, autosomal recessive (RRS)
OMIM ID	268310
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ROR2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-08-28 18:26:52 +02:00 (CEST)
Date last edited	N/A