Preferred Name |
carnitine-acylcarnitine translocase deficiency |
Synonyms |
SMP:00517 |
Definitions |
A rare autosomal recessive condition resulting from alteration in long-fatty acid oxidation and due to defects in the SLC25A20 gene. |
ID |
http://purl.obolibrary.org/obo/PW_0002506 |
created_by |
VPetri |
creation_date |
2016-02-12T08:39:07Z |
definition |
A rare autosomal recessive condition resulting from alteration in long-fatty acid oxidation and due to defects in the SLC25A20 gene. |
has_obo_namespace |
pathway |
has_related_synonym |
SMP:00517 |
id |
PW:0002506 |
label |
carnitine-acylcarnitine translocase deficiency |
notation |
PW:0002506 |
prefLabel |
carnitine-acylcarnitine translocase deficiency |
treeView | |
subClassOf |