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Exophthalmic Ophthalmoplegia

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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Exophthalmic Ophthalmoplegia is related to graves disease 1 and kearns-sayre syndrome, and has symptoms including ophthalmoplegia An important gene associated with Exophthalmic Ophthalmoplegia is KCNJ18 (Potassium Inwardly Rectifying Channel Subfamily J Member 18). Affiliated tissues include thyroid and breast.
Related ID：
MALACARDS：EXP003

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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2
27
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EXP003

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

Title
PMID
Journal
Year
IF
No Data Found!
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