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

Official abbreviation PBD13A
Name peroxisome biogenesis disorder, type 13A (PBD13A)
OMIM ID 614887
Human Phenotype Ontology Project (HPO) HPO
Inheritance AR
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PEX14
Associated tissues -
Disease features -
Remarks -