Hemifacial hypertrophy
Symptom Information:
Symptom ID: | HPO:0005323 | ||||
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) Abnormal facial shape(HPO:0001999) Facial asymmetry(HPO:0000324) Hemifacial hypertrophy(HPO:0005323) MedDRA: |
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Database Frequency: | 3 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
48,XXYY syndrome | (Orphanet:10) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Bencze syndrome | (Orphanet:1241) |