Peroxisome Biogenesis Disorder 13a (PBD13A)

Alias:

Pbd13a

Peroxisome Biogenesis Disorder, Complementation Group K

Peroxisome Biogenesis Disorder Complementation Group K

Peroxisome Biogenesis Disorder, Type 13a

Pbd-Cgk

Favorite

Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Peroxisome Biogenesis Disorder 13a, is also known as pbd13a, and has symptoms including icterus An important gene associated with Peroxisome Biogenesis Disorder 13a is PEX14 (Peroxisomal Biogenesis Factor 14). Affiliated tissues include liver and eye, and related phenotypes are seizure and hypotonia

Related ID：

MALACARDS：PRX052

OMIM：614887

MESH：D015211