Disease #05381 (PREMBL1 (lethality, embryonic, preimplantation, type 1 (PREMBL-1)), OMIM:616814)

Global Variome shared LOVD

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Official abbreviation	PREMBL1
Name	lethality, embryonic, preimplantation, type 1 (PREMBL-1)
OMIM ID	616814
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TLE6
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2018-01-26 10:24:19 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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