Abnormality of the antihelix

Symptom Information:

Symptom ID: HPO:0009738
Abnormal antihelix [HPO:0009738]
Antihelix anomaly [Orphanet:13380]
Cross references:
Orphanet:13380 "Antihelix anomaly" [Orphanet:13380]
Is a (Direct Parents):
HPO         Abnormality of the pinna
Orphanet Abnormality of the outer ear
Is a (Whole tree): HPO:
    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)
Database Frequency: 37 / 7739

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)