Pointed helix
Symptom Information:
| Symptom ID: | HPO:0100810 | ||
| Synonyms: |
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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 the helix(HPO:0011039) Pointed helix(HPO:0100810) MedDRA: |
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| Database Frequency: | 3 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| 8q22.1 microdeletion syndrome | (Orphanet:178303) |
| Craniosynostosis - fibular aplasia | (Orphanet:1533) |
| Trisomy 18 | (Orphanet:3380) |