Disease #01132 (PBD-14B;PEX-14B (peroxisome biogenesis disorder, type 14B (PBD-14B, PEX-14B)), OMIM:614920)
| Official abbreviation |
PBD-14B;PEX-14B |
| Name |
peroxisome biogenesis disorder, type 14B (PBD-14B, PEX-14B) |
| OMIM ID |
614920 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PEX11B |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
