Related MeSH Hierarchy (6)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Eye Diseases, Hereditary » Graves Ophthalmopathy
Diseases [C] » Endocrine System Diseases [C19] » Thyroid Diseases » Hyperthyroidism » Graves Disease » Graves Ophthalmopathy
Diseases [C] » Eye Diseases [C11] » Eye Diseases, Hereditary » Graves Ophthalmopathy
Diseases [C] » Eye Diseases [C11] » Orbital Diseases » Exophthalmos » Graves Disease » Graves Ophthalmopathy
Diseases [C] » Endocrine System Diseases [C19] » Thyroid Diseases » Goiter » Graves Disease » Graves Ophthalmopathy
Diseases [C] » Immune System Diseases [C20] » Autoimmune Diseases » Graves Disease » Graves Ophthalmopathy
Description
An autoimmune disorder of the EYE, occurring in patients with Graves disease. Subtypes include congestive (inflammation of the orbital connective tissue), myopathic (swelling and dysfunction of the extraocular muscles), and mixed congestive-myopathic ophthalmopathy. MeSH
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Approved Indicated Drugs (1)
Phase 4 Indicated Drugs (18)
Other Experimental Indicated Drugs (5)
Organization Involved with Phase 4 Indications (16)
Organization Involved with Phase 3 Indications (16)
Organization Involved with Phase 2 Indications (19)
Organization Involved with Phase 1 Indications (1)
Organization Involved with Other Experimental Indications (11)
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UMLS Data
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