Congenital Fibrosis of the Extraocular Muscles (FEOM)

Alias:
Congenital Fibrosis of Extraocular Muscles
Cfeom
Feom
Congenital External Ophthalmoplegia
Congenital Fibrosis Syndrome
General Fibrosis Syndrome
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Congenital Fibrosis of the Extraocular Muscles, also known as congenital fibrosis of extraocular muscles, is related to fibrosis of extraocular muscles, congenital, 1 and tukel syndrome, and has symptoms including ophthalmoplegia An important gene associated with Congenital Fibrosis of the Extraocular Muscles is TUBA1A (Tubulin Alpha 1a), and among its related pathways/superpathways are Signal Transduction and Nervous system development. The drugs Immunologic Factors and Growth Inhibitors have been mentioned in the context of this disorder. Affiliated tissues include eye and brain, and related phenotypes are ptosis and strabismus
Related ID:
MESH:C580012

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
AD
Newborn
1-9/1000000
46
298
23

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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No data available

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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IF
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