Osteoporosis-Pseudoglioma Syndrome (OPPG)

Alias:
Oppg
Ocular Form of Osteogenesis Imperfecta
Osteoporosis with Pseudoglioma
Osteogenesis Imperfecta, Ocular Form
Ops
Osteogenesis Imperfecta Ocular Form
Osteoporosis Pseudoglioma Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Osteoporosis-Pseudoglioma Syndrome, also known as oppg, is related to retinal detachment and persistent hyperplastic primary vitreous. An important gene associated with Osteoporosis-Pseudoglioma Syndrome is LRP5 (LDL Receptor Related Protein 5), and among its related pathways/superpathways are Signal Transduction and RAF/MAP kinase cascade. The drugs Sodium citrate and Lithium carbonate have been mentioned in the context of this disorder. Affiliated tissues include bone and eye, and related phenotypes are osteoporosis and increased susceptibility to fractures
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Child
--
20
260
22

Medical Symptom

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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Related Drugs

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No data available

Disease Model

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Name
MGI
Related Gene
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Publications
No data available

References Literature

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