Disease #01703 (PBD2A (peroxisome biogenesis disorder, type 2A (PBD2A)), OMIM:214110)
Official abbreviation |
PBD2A |
Name |
peroxisome biogenesis disorder, type 2A (PBD2A) |
OMIM ID |
214110 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
AR |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
PEX5 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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