Disease #06699 (PBD10B (?Peroxisome biogenesis disorder 10B), OMIM:617370)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curators: Maria Paola Lombardi and Raoul Hennekam

Official abbreviation	PBD10B
Name	?Peroxisome biogenesis disorder 10B
OMIM ID	617370
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PEX3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	N/A

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