Abnormality of earlobe
Symptom Information:
Symptom ID: | HPO:0000363 | |||
Synonyms: |
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Quality: | ||||
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 ear(HPO:0000598) Abnormality of the outer ear(HPO:0000356) Abnormality of the pinna(HPO:0000377) Abnormality of earlobe(HPO:0000363) MedDRA: |
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Database Frequency: | 4 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Beckwith-Wiedemann syndrome due to CDKN1C mutation | (Orphanet:231120) |
Costello syndrome | (Orphanet:3071) |
Lethal hemolytic anemia - genital anomalies | (Orphanet:1046) |
Polysyndactyly | (Orphanet:93338) |