Disease #04637 (WSMN (Waisman syndrome? (WSMN)), OMIM:311510)

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	Curator: Johan T. den Dunnen

Official abbreviation	WSMN
Name	Waisman syndrome? (WSMN)
OMIM ID	311510
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RAB39B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:23 +02:00 (CEST)
Date last edited	N/A