Disease #00437
Official abbreviation |
CACTD |
Name |
CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY;CACTD |
OMIM ID |
212138 |
Human Phenotype Ontology Project (HPO) |
HPO |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
SLC25A20 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
|