Disease #01703 (PBD2A (peroxisome biogenesis disorder, type 2A (PBD2A)), OMIM:214110)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	PBD2A
Name	peroxisome biogenesis disorder, type 2A (PBD2A)
OMIM ID	214110
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PEX5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-09-07 10:38:22 +02:00 (CEST)

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