Disease #03776 (PBD11B (peroxisome biogenesis disorder, type 11B (PBD-11B)), OMIM:614885)
Official abbreviation |
PBD11B |
Name |
peroxisome biogenesis disorder, type 11B (PBD-11B) |
OMIM ID |
614885 |
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 |
PEX13 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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