Crimped helix
Symptom Information:
Symptom ID: | HPO:0011262 | ||||||
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 the helix(HPO:0011039) Crimped helix(HPO:0011262) MedDRA: |
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Database Frequency: | 12 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
20p12.3 microdeletion syndrome | (Orphanet:261295) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cutis gyrata - acanthosis nigricans - craniosynostosis | (Orphanet:1555) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Intellectual deficit, X-linked, Stevenson type | (Orphanet:85325) |
Kleefstra syndrome | (Orphanet:261494) |
Monosomy 13q14 | (Orphanet:1587) |
Oculo-palato-cerebral syndrome | (Orphanet:2714) |
Perlman syndrome | (Orphanet:2849) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Spondylo-ocular syndrome | (Orphanet:85194) |
Toriello-Carey syndrome | (Orphanet:3338) |