Disease #00466
Official abbreviation |
CPT II |
Name |
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE;CPT2 |
OMIM ID |
600649 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 2 genes |
, CPT2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|