Disease #03764 (PBD6B (peroxisome biogenesis disorder, type 6B (PBD-6B)), OMIM:614871)
Official abbreviation |
PBD6B |
Name |
peroxisome biogenesis disorder, type 6B (PBD-6B) |
OMIM ID |
614871 |
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 |
PEX10 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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