Conjunctivitis
Symptom Information:
Symptom ID: | HPO:0000509 | ||||||||||||||||||||||||||||||||||||||
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 morphology(HPO:0012372) Abnormality of the conjunctiva(HPO:0000502) Conjunctivitis(HPO:0000509) Abnormal eye physiology(HPO:0012373) Inflammatory abnormality of the eye(HPO:0100533) Conjunctivitis(HPO:0000509) MedDRA: Eye disorders(MedDRA:10015919) Ocular infections, irritations and inflammations(MedDRA:10021877) Conjunctival infections, irritations and inflammations(MedDRA:10010722) Conjunctivitis(HPO:0000509) |
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Database Frequency: | 47 / 7739 | ||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ADULT syndrome | (Orphanet:978) |
AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE | (OMIM:601495) |
AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE | (OMIM:612692) |
AGAMMAGLOBULINEMIA, X-LINKED | (OMIM:300755) |
Ankyloblepharon - ectodermal defects - cleft lip/palate | (Orphanet:1071) |
Autosomal agammaglobulinemia | (Orphanet:33110) |
Biotinidase deficiency | (Orphanet:79241) |
CANDLE syndrome | (Orphanet:325004) |
Congenital erythropoietic porphyria | (Orphanet:79277) |
Crouzon disease | (Orphanet:207) |
DE SANCTIS-CACCHIONE SYNDROME | (OMIM:278800) |
DERMATITIS, ATOPIC | (OMIM:603165) |
Familial cold urticaria | (Orphanet:47045) |
Hidrotic ectodermal dysplasia | (Orphanet:189) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hypoplasminogenemia | (Orphanet:722) |
ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS | (OMIM:242150) |
IMMUNODEFICIENCY, COMMON VARIABLE, 1 | (OMIM:607594) |
IMMUNODEFICIENCY, COMMON VARIABLE, 2 | (OMIM:240500) |
IMMUNODEFICIENCY, COMMON VARIABLE, 3 | (OMIM:613493) |
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
JMP syndrome | (Orphanet:324999) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT | (OMIM:612843) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED | (OMIM:308800) |
Kawasaki disease | (Orphanet:2331) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
LACRIMAL DUCT DEFECT | (OMIM:149700) |
Lymphedema - distichiasis | (Orphanet:33001) |
Mandibulofacial dysostosis - macroblepharon - macrostomia | (Orphanet:357158) |
Muckle-Wells syndrome | (Orphanet:575) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Normocalcemic tumoral calcinosis | (Orphanet:306658) |
Poikiloderma with neutropenia | (Orphanet:221046) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Proteasome disability syndrome | (Orphanet:324977) |
Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
Severe combined immunodeficiency due to complete RAG1/2 deficiency | (Orphanet:331206) |
Severe generalized recessive dystrophic epidermolysis bullosa | (Orphanet:79408) |
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia | (Orphanet:632) |
Transketolase deficiency | (ORPHA:488618) |
Tyrosinemia type 2 | (Orphanet:28378) |
Xeroderma pigmentosum complementation group A | (Orphanet:276249) |
Xeroderma pigmentosum complementation group C | (Orphanet:276255) |
Xeroderma pigmentosum complementation group D | (Orphanet:276258) |
Xeroderma pigmentosum complementation group E | (Orphanet:276261) |
Xeroderma pigmentosum variant | (Orphanet:90342) |
Xeroderma pigmentosum/Cockayne syndrome complex | (Orphanet:220295) |