Disease #03768 (PBD8A (peroxisome biogenesis disorder, type 8A (PBD-8A)), OMIM:614876)
Official abbreviation |
PBD8A |
Name |
peroxisome biogenesis disorder, type 8A (PBD-8A) |
OMIM ID |
614876 |
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 |
PEX16 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|