Uveitis
Symptom Information:
Symptom ID: | HPO:0000554 | |||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the eye(HPO:0000478) Abnormal eye physiology(HPO:0012373) Inflammatory abnormality of the eye(HPO:0100533) Uveitis(HPO:0000554) Abnormal eye morphology(HPO:0012372) Abnormality of the globe(HPO:0012374) Abnormality of the uvea(HPO:0000553) Uveitis(HPO:0000554) MedDRA: Immune system disorders(MedDRA:10021428) Autoimmunity(HPO:0002960) Autoimmune disorders NEC(MedDRA:10027657) Uveitis(HPO:0000554) |
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Database Frequency: | 10 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant neovascular inflammatory vitreoretinopathy | (Orphanet:329211) |
Behçet disease | (Orphanet:117) |
Blau syndrome | (Orphanet:90340) |
Congenital blindness due to retinal non-attachment | (Orphanet:300337) |
Incontinentia pigmenti | (Orphanet:464) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
SARCOIDOSIS, SUSCEPTIBILITY TO, 1 | (OMIM:181000) |
Transketolase deficiency | (ORPHA:488618) |
Tubulointerstitial nephritis and uveitis syndrome | (Orphanet:91500) |
Tyrosinemia type 2 | (Orphanet:28378) |