Disease #03765 (PBD7A (peroxisome biogenesis disorder, type 7A (PBD-7A)), OMIM:614872)
Official abbreviation |
PBD7A |
Name |
peroxisome biogenesis disorder, type 7A (PBD-7A) |
OMIM ID |
614872 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
PEX26 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|