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Peroxisome Biogenesis Disorder 10b (PBD10B)

Alias:
Pbd10b
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Peroxisome Biogenesis Disorder 10b, is also known as pbd10b. An important gene associated with Peroxisome Biogenesis Disorder 10b is PEX3 (Peroxisomal Biogenesis Factor 3). Affiliated tissues include kidney, and related phenotypes are hyperreflexia and nystagmus
Related ID：
MALACARDS：PRX089
OMIM：617370
MESH：D052919

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
--
1
5
1
PRX089

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

Name
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
Year
IF
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