Disease #03760 (PBD5B (peroxisome biogenesis disorder, type 5B (PBD-5B)), OMIM:614867)

Official abbreviation PBD5B
Name peroxisome biogenesis disorder, type 5B (PBD-5B)
OMIM ID 614867
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PEX2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)