Peroxisome Biogenesis Disorder 6a (PBD6A)

Alias:

Peroxisome Biogenesis Disorder, Complementation Group 7

Pbd6a

Peroxisome Biogenesis Disorder Complementation Group 7

Peroxisome Biogenesis Disorder Complementation Group B

Peroxisome Biogenesis Disorder, Type 6a

Pbd-Cg7

Pbd-Cgb

Cg7

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Peroxisome Biogenesis Disorder 6a, also known as peroxisome biogenesis disorder, complementation group 7, is related to peroxisome biogenesis disorder 6b. An important gene associated with Peroxisome Biogenesis Disorder 6a is PEX10 (Peroxisomal Biogenesis Factor 10). Affiliated tissues include liver and eye, and related phenotypes are seizure and hypotonia

Related ID：

MALACARDS：PRX051

OMIM：614870

MESH：D015211