Disease #03777 (PBD-12A (peroxisome biogenesis disorder, type 12A (PBD-12A)), OMIM:614886)

Official abbreviation PBD-12A
Name peroxisome biogenesis disorder, type 12A (PBD-12A)
OMIM ID 614886
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PEX19
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A

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