Disease #05380 (PREMBL2 (lethality, embryonic, preimplantation, type 2 (PREMBL-2)), OMIM:617234)

Official abbreviation	PREMBL2
Name	lethality, embryonic, preimplantation, type 2 (PREMBL-2)
OMIM ID	617234
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PADI6
Associated tissues	-
Disease features	autosomal recessive
Remarks	-
Date created	2018-01-26 10:17:36 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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