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
|