Euthyroid Graves orbitopathy
Synonyms: Euthyroid Graves ophthalmopathy
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
A rare ophthalmic disorder characterized by clinical signs of Graves orbitopathy (i. e. unilateral or bilateral lid retraction, exophthalmos, soft tissue involvement, restrictive myopathy, and/or optic neuropathy) with normal thyroid function and without any signs of hyperthyroidism. Laboratory examination typically reveals low serum levels of thyroid-stimulating hormone receptor autoantibodies.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Euthyroid Graves orbitopathy | Euthyroid Graves ophthalmopathy |
| fr | Orbitopathie euthyroïdienne | Ophtalmopathie euthyroïdienne |
| de | Euthyreote Graves-Orbitopathie | Euthyreote endokrine Ophthalmopathie Graves |
| es | Orbitopatía eutiroidea de Graves | Oftalmopatía eutiroidea de Graves |
| it | Orbitopatia eutiroidea di Graves | |
| nl | Euthyroïde Graves' orbitopathie | Euthyroïde Graves' oftalmopathie |
| pt | Orbitopatia da doença de Graves eutiroideia | |
| pl | Orbitopatia Gravesa | Oftalmopatia Gravesa |
| cs | Euthyroidní Gravesova orbitopatie | Euthyroid Graves ophthalmopathy · Euthyroidní Gravesova oftalmopatie |
| uk | Еутиреоїдна орбітопатія Грейвса | Еутиреоїдна офтальмопатія Грейвса |
| zh | 甲状腺肿相关眼病 | 甲状腺肿相关眼病 |
| tr | Ötiroid Graves orbitopati | Ötiroid-Graves oftalmopatisi |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | H05.2 | NTBT | attributed | validated |
| ICD-11 | 9A20.00 | NTBT | attributed | validated |
| MONDO | 0018756 | E | validated | |
| UMLS | C5680004 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:519329Rare disorder involving multiple structures of the eye
rare ophthalmic disorders
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/466682
- This record as JSON: /data/d/466682.json