Inflammatory abnormality of the eye
Symptom Information:
Symptom ID: | HPO:0100533 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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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) MedDRA: |
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Database Frequency: | 70 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
Aniridia | (Orphanet:77) |
Autosomal agammaglobulinemia | (Orphanet:33110) |
Biotinidase deficiency | (Orphanet:79241) |
Blau syndrome | (Orphanet:90340) |
CINCA syndrome | (Orphanet:1451) |
Chronic granulomatous disease | (Orphanet:379) |
Cogan syndrome | (Orphanet:1467) |
Congenital non-bullous ichthyosiform erythroderma | (Orphanet:79394) |
Corneal anesthesia - deafness - intellectual deficit | (Orphanet:1051) |
Crimean-Congo hemorrhagic fever | (Orphanet:99827) |
Crouzon disease | (Orphanet:207) |
Crouzon syndrome - acanthosis nigricans | (Orphanet:93262) |
Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
Dyskeratosis congenita | (Orphanet:1775) |
EEC syndrome | (Orphanet:1896) |
Ectodermal dysplasia syndrome | (Orphanet:79373) |
Enthesitis-related arthritis | (Orphanet:85438) |
FLOTCH syndrome | (Orphanet:2045) |
Familial cold urticaria | (Orphanet:47045) |
Felty syndrome | (Orphanet:47612) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Holocarboxylase synthetase deficiency | (Orphanet:79242) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
Immunoglobulin A vasculitis | (Orphanet:761) |
Incontinentia pigmenti | (Orphanet:464) |
Isolated agammaglobulinemia | (Orphanet:229717) |
Junctional epidermolysis bullosa | (Orphanet:305) |
Juvenile idiopathic arthritis | (Orphanet:92) |
Juvenile xanthogranuloma | (Orphanet:158000) |
KID syndrome | (Orphanet:477) |
Kawasaki disease | (Orphanet:2331) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Kindler syndrome | (Orphanet:2908) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Lassa fever | (Orphanet:99824) |
Leukonychia totalis | (Orphanet:2387) |
Lyell syndrome | (Orphanet:537) |
Lyme disease | (Orphanet:91546) |
Lymphedema - distichiasis | (Orphanet:33001) |
Majeed syndrome | (Orphanet:77297) |
Microscopic polyangiitis | (Orphanet:727) |
Muckle-Wells syndrome | (Orphanet:575) |
Mucous membrane pemphigoid | (Orphanet:46486) |
Multiple carboxylase deficiency | (Orphanet:148) |
Nodular non-suppurative panniculitis | (Orphanet:33577) |
Odonto-onycho-dermal dysplasia | (Orphanet:2721) |
Oligoarticular juvenile arthritis | (Orphanet:85410) |
Polyarteritis nodosa | (Orphanet:767) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Reactive arthritis | (Orphanet:29207) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Relapsing polychondritis | (Orphanet:728) |
Scrub typhus | (Orphanet:83317) |
Sjögren-Larsson syndrome | (Orphanet:816) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Stickler syndrome | (Orphanet:828) |
Sweet syndrome | (Orphanet:3243) |
TRAPS syndrome | (Orphanet:32960) |
Takayasu arteritis | (Orphanet:3287) |
Tumoral calcinosis | (Orphanet:53715) |
Tyrosinemia type 2 | (Orphanet:28378) |
Whipple disease | (Orphanet:3452) |
Wiskott-Aldrich syndrome | (Orphanet:906) |
X-linked agammaglobulinemia | (Orphanet:47) |
Xeroderma pigmentosum | (Orphanet:910) |