Thickened helices
Symptom Information:
Symptom ID: | HPO:0000391 | |||||
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) Thickened helices(HPO:0000391) MedDRA: |
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Database Frequency: | 8 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
22q11.2 microduplication syndrome | (Orphanet:1727) |
GELEOPHYSIC DYSPLASIA 1 | (OMIM:231050) |
Geleophysic dysplasia | (Orphanet:2623) |
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA | (OMIM:608624) |
NOONAN SYNDROME 7 | (OMIM:613706) |
Noonan syndrome | (Orphanet:648) |
Rabson-Mendenhall syndrome | (Orphanet:769) |