Disease #00012 (CPT1D (carnitine palmitoyltransferase 1 dificiency), OMIM:600528)
Official abbreviation |
CPT1D |
Name |
carnitine palmitoyltransferase 1 dificiency |
OMIM ID |
600528 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 0 genes |
- |
Associated tissues |
liver |
Disease features |
- |
Remarks |
- |
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