Disease #02369 (PBD-1B (peroxisome biogenesis disorder, type 1B (PBD-1B, (NALD/IRD))), OMIM:601539)
| Official abbreviation |
PBD-1B |
| Name |
peroxisome biogenesis disorder, type 1B (PBD-1B, (NALD/IRD)) |
| OMIM ID |
601539 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PEX1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|