Pathway Ontology / 通路本体

Last uploaded: September 7, 2023
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

http://purl.obolibrary.org/obo/PW_0001643

subClassOf

http://purl.obolibrary.org/obo/PW_0001643

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