Inflammatory abnormality of the eye

Symptom Information:

Symptom ID: HPO:0100533
Ocular inflammation [HPO:0100533]
Cross references:
Is a (Direct Parents):
HPO         Abnormal eye physiology
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye physiology(HPO:0012373)
             Inflammatory abnormality of the eye(HPO:0100533)
Database Frequency: 70 / 7739

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)