Osteogenesis Imperfecta, Type Xviii (OI18)

Alias:
Oi18
Osteogenesis Imperfecta, Type 18
Osteogenesis Imperfecta Type 18
Osteogenesis Imperfecta 18
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Osteogenesis Imperfecta, Type Xviii, also known as oi18, is related to mediastinitis and central sleep apnea. An important gene associated with Osteogenesis Imperfecta, Type Xviii is TENT5A (Terminal Nucleotidyltransferase 5A), and among its related pathways/superpathways is Anti-diabetic Drug Potassium Channel Inhibitors Pathway, Pharmacodynamics. Affiliated tissues include bone and cortex, and related phenotypes are abnormality of the dentition and recurrent fractures
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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5
64
1

Medical Symptom

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Description
HPO Frequency
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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
Strain of Origin
Publications
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References Literature

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