Periorbital fullness
Symptom Information:
Symptom ID: | HPO:0000629 | |||||||||||||||||||||||||||||||
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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the periorbital region(HPO:0000606) Periorbital fullness(HPO:0000629) MedDRA: Eye disorders(MedDRA:10015919) Ocular infections, irritations and inflammations(MedDRA:10021877) Lid, lash and lacrimal infections, irritations and inflammations(MedDRA:10024445) Periorbital fullness(HPO:0000629) Eye disorders NEC(MedDRA:10015917) Ocular disorders NEC(MedDRA:10030032) Periorbital fullness(HPO:0000629) |
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Database Frequency: | 13 / 7739 | |||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION | (OMIM:204850) |
Distal monosomy 3p | (Orphanet:1620) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23 | (OMIM:615859) |
FOCAL FACIAL DERMAL DYSPLASIA 3, SETLEIS TYPE | (OMIM:227260) |
Fabry disease | (Orphanet:324) |
Hypotrichosis - lymphedema - telangiectasia | (Orphanet:69735) |
Intellectual deficit, X-linked, Shashi type | (Orphanet:85286) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Large congenital melanocytic nevus | (Orphanet:626) |
Non-progressive cerebellar ataxia with intellectual deficit | (Orphanet:314647) |
Sialuria | (Orphanet:3166) |
Suarez-Stickler syndrome | (Orphanet:166277) |
Williams syndrome | (Orphanet:904) |