Aplasia/Hypoplasia of the external ear
Symptom Information:
| Symptom ID: | HPO:0008772 | ||||||
| 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) Aplasia/Hypoplasia of the ear(HPO:0008771) Aplasia/Hypoplasia of the external ear(HPO:0008772) Abnormality of the outer ear(HPO:0000356) Aplasia/Hypoplasia of the external ear(HPO:0008772) MedDRA: |
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| Database Frequency: | 67 / 7739 | ||||||
| Resource: |
All diseases associated with this symptom:
| 1p36 deletion syndrome | (Orphanet:1606) |
| 20p12.3 microdeletion syndrome | (Orphanet:261295) |
| 3-hydroxyisobutyric aciduria | (Orphanet:939) |
| Ablepharon macrostomia syndrome | (Orphanet:920) |
| Acro-pectoro-renal dysplasia | (Orphanet:956) |
| Acrofacial dysostosis, Rodriguez type | (Orphanet:1788) |
| Agnathia - holoprosencephaly - situs inversus | (Orphanet:990) |
| Aspartylglucosaminuria | (Orphanet:93) |
| Atrioventricular defect - blepharophimosis -radial defects | (Orphanet:1352) |
| Auriculoosteodysplasia | (Orphanet:114) |
| Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
| Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
| CHARGE syndrome | (Orphanet:138) |
| Camptodactyly syndrome, Guadalajara type 1 | (Orphanet:1327) |
| Conductive deafness - malformed external ear | (Orphanet:3216) |
| Coxoauricular syndrome | (Orphanet:1508) |
| Craniosynostosis, Herrmann-Opitz type | (Orphanet:2145) |
| Crossed polysyndactyly | (Orphanet:2935) |
| Cryptomicrotia - brachydactyly - excess fingertip arch | (Orphanet:1547) |
| Deafness - ear malformation - facial palsy | (Orphanet:3232) |
| Deafness with labyrinthine aplasia, microtia, and microdontia | (Orphanet:90024) |
| Diabetic embryopathy | (Orphanet:1926) |
| Disorder of sex development - intellectual deficit | (Orphanet:2983) |
| Distal monosomy 17q | (Orphanet:1597) |
| Distal monosomy 9p | (Orphanet:1642) |
| Dysmorphism - short stature - deafness - disorder of sex development | (Orphanet:2282) |
| Ear-patella-short stature syndrome | (Orphanet:2554) |
| Embryofetopathy due to oral anticoagulant therapy | (Orphanet:1914) |
| Familial visceral myopathy | (Orphanet:2604) |
| Femoral-facial syndrome | (Orphanet:1988) |
| Fraser syndrome | (Orphanet:2052) |
| Goldenhar syndrome | (Orphanet:374) |
| Gonadal dysgenesis, XY type - associated anomalies | (Orphanet:1770) |
| Hand-foot-genital syndrome | (Orphanet:2438) |
| Hennekam-Beemer syndrome | (Orphanet:2135) |
| Holoprosencephaly - radial heart renal anomalies | (Orphanet:3186) |
| Hypertelorism-microtia-facial clefting syndrome | (Orphanet:2213) |
| Intellectual deficit - myopathy - short stature - endocrine defect | (Orphanet:3068) |
| Isotretinoin syndrome | (Orphanet:2305) |
| Isotretinoin-like syndrome | (Orphanet:2306) |
| Lambert syndrome | (Orphanet:1296) |
| Lethal restrictive dermopathy | (Orphanet:1662) |
| Microphthalmia - microtia - fetal akinesia | (Orphanet:2547) |
| Microtia - eye coloboma - imperforation of the nasolacrimal duct | (Orphanet:139450) |
| Mosaic trisomy 14 | (Orphanet:1703) |
| Mycophenolate mofetil embryopathy | (Orphanet:268249) |
| Nager syndrome | (Orphanet:245) |
| Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
| Oculoauriculovertebral spectrum with radial defects | (Orphanet:2549) |
| Orofaciodigital syndrome type 4 | (Orphanet:2753) |
| Patterson-Stevenson-Fontaine syndrome | (Orphanet:2439) |
| Peters-plus syndrome | (Orphanet:709) |
| Phocomelia - ectrodactyly - deafness - sinus arrhythmia | (Orphanet:2878) |
| Pseudoprogeria syndrome | (Orphanet:2985) |
| Saethre-Chotzen syndrome | (Orphanet:794) |
| Scalp-ear-nipple syndrome | (Orphanet:2036) |
| Short stature - craniofacial anomalies - genital hypoplasia | (Orphanet:2994) |
| Teebi-Shaltout syndrome | (Orphanet:3291) |
| Tetraamelia - multiple malformations | (Orphanet:3301) |
| Thalidomide embryopathy | (Orphanet:3312) |
| Townes-Brocks syndrome | (Orphanet:857) |
| Treacher-Collins syndrome | (Orphanet:861) |
| Trisomy 1q | (Orphanet:261344) |
| VACTERL with hydrocephalus | (Orphanet:3412) |
| Verloove Vanhorick-Brubakk syndrome | (Orphanet:3429) |
| Wolf-Hirschhorn syndrome | (Orphanet:280) |
| Yunis-Varon syndrome | (Orphanet:3472) |