Disease #00126 (SCKL (Seckel syndrome (SCKL)), OMIM:210600)

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	Curator: Johan T. den Dunnen

Official abbreviation	SCKL
Name	Seckel syndrome (SCKL)
OMIM ID	210600
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 6 genes	ATR, CENPJ, CEP152, CEP63, NIN, RBBP8
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-05-07 07:32:22 +02:00 (CEST)
Date last edited	N/A