Disease #06556 (SCKL9 (Seckel syndrome, type 9), OMIM:616777)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SCKL9
Name	Seckel syndrome, type 9
OMIM ID	616777
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TRAIP
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2023-03-14 15:40:17 +01:00 (CET)

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