Disease #01956 (CPTD1A (carnitine palmitoyltransferase deficiency, type IA), OMIM:255120)
| Official abbreviation |
CPTD1A |
| Name |
carnitine palmitoyltransferase deficiency, type IA |
| OMIM ID |
255120 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
CPT1A |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2024-11-14 14:49:30 +01:00 (CET) |
Individuals
|