Disease #00271 (SCKL-2 (Seckel syndrome, type 2 (SCKL-2)), OMIM:606744)

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	Curator: Johan T. den Dunnen

Official abbreviation	SCKL-2
Name	Seckel syndrome, type 2 (SCKL-2)
OMIM ID	606744
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RBBP8
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-11-22 15:16:48 +01:00 (CET)
Date last edited	N/A