Carnitine Palmitoyltransferase Ii Deficiency, Myopathic, Stress-Induced (CPT2D)

Alias:

Carnitine Palmitoyl Transferase Ii Deficiency, Myopathic Form

Carnitine Palmitoyltransferase Ii Deficiency, Adult-Onset

Carnitine Palmitoyltransferase Ii Deficiency, Myopathic

Cpt Ii Deficiency, Myopathic

Cpt2 Deficiency, Late-Onset

Carnitine Palmitoyltransferase 2 Deficiency, Myopathic, Stress-Induced

Carnitine Palmitoyl Transferase Deficiency Type 2, Adult-Onset Form

Carnitine Palmitoyl Transferase Deficiency Type 2, Myopathic Form

Carnitine Palmitoyl Transferase Ii Deficiency, Adult-Onset Form

Carnitine Palmitoyltransferase Ii Deficiency, Late-Onset

Carnitine Palmitoyltransferase 2 Deficiency, Late-Onset

Cpt Ii Deficiency, Myopathic, Stress-Induced

Cptii, Adult-Onset Form

Cpt2, Adult-Onset Form

Cptii, Myopathic Form

Cpt2, Myopathic Form

Cpt2d

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Carnitine Palmitoyltransferase Ii Deficiency, Myopathic, Stress-Induced, also known as carnitine palmitoyl transferase ii deficiency, myopathic form, is related to carnitine palmitoyltransferase ii deficiency, infantile and acyl-coa dehydrogenase, very long-chain, deficiency of, and has symptoms including muscle cramp, muscular stiffness and myalgia. An important gene associated with Carnitine Palmitoyltransferase Ii Deficiency, Myopathic, Stress-Induced is CPT2 (Carnitine Palmitoyltransferase 2). The drugs Glycerin and Heparin, bovine have been mentioned in the context of this disorder. Affiliated tissues include kidney and skeletal muscle, and related phenotypes are myalgia and exercise-induced myalgia

Related ID：

MALACARDS：CRN294

OMIM：255110

MESH：D008661