Periorbital edema
Symptom Information:
Symptom ID: | HPO:0100539 | ||||||||||||||||||||||||||||
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 edema(HPO:0100539) Abnormality of facial soft tissue(HPO:0011799) Facial edema(HPO:0000282) Periorbital edema(HPO:0100539) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of fluid regulation(HPO:0011032) Edema(HPO:0000969) Facial edema(HPO:0000282) Periorbital edema(HPO:0100539) MedDRA: Eye disorders(MedDRA:10015919) Eye disorders NEC(MedDRA:10015917) Ocular disorders NEC(MedDRA:10030032) Periorbital edema(HPO:0100539) Ocular infections, irritations and inflammations(MedDRA:10021877) Lid, lash and lacrimal infections, irritations and inflammations(MedDRA:10024445) Periorbital edema(HPO:0100539) |
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Database Frequency: | 8 / 7739 | ||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION | (OMIM:204850) |
Gaucher disease type 1 | (Orphanet:77259) |
Hennekam syndrome | (Orphanet:2136) |
Hypotrichosis - lymphedema - telangiectasia | (Orphanet:69735) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Multiple sulfatase deficiency | (Orphanet:585) |
Non-progressive cerebellar ataxia with intellectual deficit | (Orphanet:314647) |
TRAPS syndrome | (Orphanet:32960) |