Disease #00274 (SCKL-5 (Seckel syndrome, type 5 (SCKL-5)), OMIM:613823)

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	Curator: Johan T. den Dunnen

Official abbreviation	SCKL-5
Name	Seckel syndrome, type 5 (SCKL-5)
OMIM ID	613823
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CEP152
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-11-22 15:19:05 +01:00 (CET)
Date last edited	N/A