Combined Oxidative Phosphorylation Deficiency 29 (COXPD29)

Alias:

Coxpd29

Combined Oxidative Phosphorylation Deficiency, Type 29

Combined Oxidative Phosphorylation Defect Type 29

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Combined Oxidative Phosphorylation Deficiency 29, is also known as coxpd29. An important gene associated with Combined Oxidative Phosphorylation Deficiency 29 is TXN2 (Thioredoxin 2). Affiliated tissues include brain and skeletal muscle, and related phenotypes are abnormal autonomic nervous system physiology and retinopathy

Related ID：

MALACARDS：CMB079

OMIM：616811

MESH：D028361