Keratitis
Symptom Information:
Symptom ID: | HPO:0000491 | ||||||||||||||||||||||||||||||||
Synonyms: |
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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 globe(HPO:0012374) Abnormality of the anterior segment of the globe(HPO:0004328) Abnormality of the cornea(HPO:0000481) Abnormality of corneal epithelium(HPO:0011495) Keratitis(HPO:0000491) Abnormal eye physiology(HPO:0012373) Inflammatory abnormality of the eye(HPO:0100533) Keratitis(HPO:0000491) MedDRA: Eye disorders(MedDRA:10015919) Ocular infections, irritations and inflammations(MedDRA:10021877) Corneal infections, oedemas and inflammations(MedDRA:10011021) Keratitis(HPO:0000491) |
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Database Frequency: | 21 / 7739 | ||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant keratitis | (Orphanet:2334) |
Corneal anesthesia - deafness - intellectual deficit | (Orphanet:1051) |
DE SANCTIS-CACCHIONE SYNDROME | (OMIM:278800) |
Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
Hereditary sensory and autonomic neuropathy type 4 | (Orphanet:642) |
Incontinentia pigmenti | (Orphanet:464) |
KERATITIS FUGAX HEREDITARIA | (OMIM:148200) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT | (OMIM:612843) |
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED | (OMIM:308800) |
Keratosis follicularis spinulosa decalvans | (Orphanet:2340) |
Mandibulofacial dysostosis - macroblepharon - macrostomia | (Orphanet:357158) |
Posterior polymorphous corneal dystrophy | (Orphanet:98973) |
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) |