Peroxisome Biogenesis Disorder 8a (PBD8A)

Alias:
Pbd8a
Peroxisome Biogenesis Disorder Complementation Group 9
Peroxisome Biogenesis Disorder Complementation Group D
Peroxisome Biogenesis Disorder, Type 8a
Pbd-Cg9
Pbd-Cgd
Cg9
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Peroxisome Biogenesis Disorder 8a, also known as pbd8a, is related to peroxisome biogenesis disorder 8b, and has symptoms including icterus An important gene associated with Peroxisome Biogenesis Disorder 8a is PEX16 (Peroxisomal Biogenesis Factor 16). Affiliated tissues include liver and eye, and related phenotypes are seizure and cataract
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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1
5
3

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
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IF
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