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

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 0
Phenotype entries for this disease 0
Associated with 1 gene PEX3
Associated tissues -
Disease features -
Remarks -