MeSH Treeview
Query OMIM entry list
609384
CFEOM3B
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B
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Nervous System Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Ophthalmoplegia
Neurologic Manifestations
Paralysis
Ophthalmoplegia
Eye Diseases
Eyelid Diseases
Blepharoptosis
Ocular Motility Disorders
Ophthalmoplegia
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Translocation, Genetic
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Fibrosis
Signs and Symptoms
Neurologic Manifestations
Paralysis
Ophthalmoplegia
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