Disease #00273 (SCKL4 (Seckel syndrome, type 4 (SCKL-4)), OMIM:613676)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

	Curator: Global Variome, with Curator vacancy

Official abbreviation	SCKL4
Name	Seckel syndrome, type 4 (SCKL-4)
OMIM ID	613676
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CENPJ
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-11-22 15:18:18 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.