Disease #03778 (PBD13A (peroxisome biogenesis disorder, type 13A (PBD13A)), OMIM:614887)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	PBD13A
Name	peroxisome biogenesis disorder, type 13A (PBD13A)
OMIM ID	614887
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PEX14
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-09-04 17:19:39 +02:00 (CEST)

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