Combined Oxidative Phosphorylation Deficiency 1 (COXPD1)

Alias:
Hepatoencephalopathy Due to Combined Oxidative Phosphorylation Defect Type 1
Coxpd1
Early Fatal Progressive Hepatoencephalopathy
Hepatoencephalopathy Due to Coxpd1
Combined Oxidative Phosphorylation Deficiency, Type 1
Hepatoencephalopathy, Early Fatal Progressive
Hepatoencephalopathy Early Fatal Progressive
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Combined Oxidative Phosphorylation Deficiency 1, also known as hepatoencephalopathy due to combined oxidative phosphorylation defect type 1, is related to combined oxidative phosphorylation deficiency 39 and combined oxidative phosphorylation deficiency 13, and has symptoms including muscle spasticity and stiffness. An important gene associated with Combined Oxidative Phosphorylation Deficiency 1 is GFM1 (G Elongation Factor Mitochondrial 1), and among its related pathways/superpathways are Metabolism of proteins and Peptide chain elongation. The drugs Rifaximin and Gastrointestinal Agents have been mentioned in the context of this disorder. Affiliated tissues include liver and brain, and related phenotypes are hypertonia and cholestasis
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
<1/1000000
12
58
12

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
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IF
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