Abnormality of the antihelix
Symptom Information:
| Symptom ID: | HPO:0009738 | ||||
| Synonyms: |
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| 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) MedDRA: |
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| Database Frequency: | 37 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| 14q12 microdeletion syndrome | (Orphanet:261144) |
| 8q22.1 microdeletion syndrome | (Orphanet:178303) |
| Acrofacial dysostosis, Weyers type | (Orphanet:952) |
| Alopecia - contractures - dwarfism - intellectual deficit | (Orphanet:1005) |
| Blepharophimosis-intellectual deficit syndrome, SBBYS type | (Orphanet:3047) |
| CHARGE syndrome | (Orphanet:138) |
| Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
| Craniosynostosis, Herrmann-Opitz type | (Orphanet:2145) |
| Deafness - ear malformation - facial palsy | (Orphanet:3232) |
| Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
| Distal monosomy 9p | (Orphanet:1642) |
| Dubowitz syndrome | (Orphanet:235) |
| Flat face - microstomia - ear anomaly | (Orphanet:1968) |
| Holoprosencephaly | (Orphanet:2162) |
| Intellectual deficit - balding - patella luxation - acromicria | (Orphanet:3041) |
| Intellectual deficit - polydactyly - uncombable hair | (Orphanet:3082) |
| Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
| Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
| Monosomy 18p | (Orphanet:1598) |
| Monosomy 9p | (Orphanet:261112) |
| Mosaic trisomy 8 | (Orphanet:96061) |
| Nephrogenic diabetes insipidus - intracranial calcification | (Orphanet:3145) |
| Non-distal trisomy 13q | (Orphanet:1702) |
| Oto-onycho-peroneal syndrome | (Orphanet:2793) |
| Otofaciocervical syndrome | (Orphanet:2792) |
| Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
| Ring chromosome 10 | (Orphanet:1438) |
| Scalp-ear-nipple syndrome | (Orphanet:2036) |
| Short rib-polydactyly syndrome | (Orphanet:1505) |
| Spondylo-ocular syndrome | (Orphanet:85194) |
| Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
| Trisomy 12p | (Orphanet:1699) |
| Trisomy 13 | (Orphanet:3378) |
| Trisomy 20p | (Orphanet:261318) |
| Trisomy 4p | (Orphanet:1738) |
| Upper limb defect - eye and ear abnormalities | (Orphanet:2489) |
| Yunis-Varon syndrome | (Orphanet:3472) |