Prominent antihelix
Symptom Information:
Symptom ID: | HPO:0000395 | ||
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 antihelix(HPO:0009738) Prominent antihelix(HPO:0000395) MedDRA: |
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Database Frequency: | 6 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Acrofacial dysostosis, Weyers type | (Orphanet:952) |
Allan-Herndon-Dudley syndrome | (Orphanet:59) |
HOLOPROSENCEPHALY 9 | (OMIM:610829) |
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome | (Orphanet:329332) |
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE | (OMIM:613744) |
TARP syndrome | (Orphanet:2886) |