Epibulbar dermoid
Symptom Information:
Symptom ID: | HPO:0001140 | ||||||||||||
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 conjunctiva(HPO:0000502) Epibulbar dermoid(HPO:0001140) Abnormality of the globe(HPO:0012374) Abnormality of the anterior segment of the globe(HPO:0004328) Abnormality of the cornea(HPO:0000481) Epibulbar dermoid(HPO:0001140) Abnormality of the sclera(HPO:0000591) Epibulbar dermoid(HPO:0001140) MedDRA: |
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Database Frequency: | 11 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
Caudal regression sequence | (Orphanet:3027) |
Encephalocraniocutaneous lipomatosis | (Orphanet:2396) |
Familial caudal dysgenesis | (Orphanet:1768) |
Fronto-facio-nasal dysostosis | (Orphanet:1791) |
Goldenhar syndrome | (Orphanet:374) |
Proteus syndrome | (Orphanet:744) |
Proteus-like syndrome | (Orphanet:2969) |
Sirenomelia | (Orphanet:3169) |
Toriello-Lacassie-Droste syndrome | (Orphanet:3339) |
Townes-Brocks syndrome | (Orphanet:857) |