Peroxisome Biogenesis Disorder 10a (PBD10A)

Alias:

Pbd10a

Peroxisome Biogenesis Disorder, Complementation Group 12

Peroxisome Biogenesis Disorder Complementation Group 12

Peroxisome Biogenesis Disorder Complementation Group G

Peroxisome Biogenesis Disorder, Type 10a

Pbd-Cg12

Pbd-Cgg

Cg12

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Peroxisome Biogenesis Disorder 10a, is also known as pbd10a. An important gene associated with Peroxisome Biogenesis Disorder 10a is PEX3 (Peroxisomal Biogenesis Factor 3). Affiliated tissues include liver and eye, and related phenotypes are seizure and high palate

Related ID：

MALACARDS：PRX048

OMIM：614882

MESH：D015211