Abnormal location of ears
Symptom Information:
| Symptom ID: | HPO:0000357 | ||||
| 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) Abnormal location of ears(HPO:0000357) MedDRA: |
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| Database Frequency: | 328 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| 10q22.3q23.3 microdeletion syndrome | (Orphanet:276413) |
| 10q22.3q23.3 microduplication syndrome | (Orphanet:276422) |
| 15q13.3 microdeletion syndrome | (Orphanet:199318) |
| 15q14 microdeletion syndrome | (Orphanet:261190) |
| 16p11.2p12.2 microdeletion syndrome | (Orphanet:261211) |
| 16p13.11 microdeletion syndrome | (Orphanet:261236) |
| 17p11.2 microduplication syndrome | (Orphanet:1713) |
| 17p13.3 microduplication syndrome | (Orphanet:217385) |
| 17q23.1q23.2 microdeletion syndrome | (Orphanet:261279) |
| 19p13.12 microdeletion syndrome | (Orphanet:254346) |
| 1p36 deletion syndrome | (Orphanet:1606) |
| 22q11.2 deletion syndrome | (Orphanet:567) |
| 2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
| 2p21 microdeletion syndrome | (Orphanet:163693) |
| 2q31.1 microdeletion syndrome | (Orphanet:251014) |
| 2q32q33 microdeletion syndrome | (Orphanet:251019) |
| 3C syndrome | (Orphanet:7) |
| 3q29 microdeletion syndrome | (Orphanet:65286) |
| 3q29 microduplication | (Orphanet:251038) |
| 4q21 microdeletion syndrome | (Orphanet:238750) |
| 6p22 microdeletion syndrome | (Orphanet:251046) |
| 6q16 deletion syndrome | (Orphanet:171829) |
| 6q25 microdeletion syndrome | (Orphanet:251056) |
| 8q21.11 microdeletion syndrome | (Orphanet:284160) |
| 8q22.1 microdeletion syndrome | (Orphanet:178303) |
| Aarskog-Scott syndrome | (Orphanet:915) |
| Acro-cardio-facial syndrome | (Orphanet:2008) |
| Acro-oto-ocular syndrome | (Orphanet:2980) |
| Acro-renal-mandibular syndrome | (Orphanet:958) |
| Acrocraniofacial dysostosis | (Orphanet:949) |
| Acrofacial dysostosis, Catania type | (Orphanet:1786) |
| Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
| Acroosteolysis, dominant type | (Orphanet:955) |
| Agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia | (Orphanet:52055) |
| Agnathia - holoprosencephaly - situs inversus | (Orphanet:990) |
| Alopecia - contractures - dwarfism - intellectual deficit | (Orphanet:1005) |
| Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 | (Orphanet:98791) |
| Aminopterin/methotrexate embryofetopathy | (Orphanet:1908) |
| Anophthalmia plus syndrome | (Orphanet:1104) |
| Antley-Bixler syndrome | (Orphanet:83) |
| Aortic arch anomaly - peculiar facies - intellectual deficit | (Orphanet:1110) |
| Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
| Arthrogryposis multiplex congenita | (Orphanet:1037) |
| Arthrogryposis multiplex congenita - whistling face | (Orphanet:1150) |
| Auriculoocular anomalies - cleft lip | (Orphanet:71270) |
| Autosomal dominant Robinow syndrome | (Orphanet:3107) |
| Autosomal recessive Robinow syndrome | (Orphanet:1507) |
| Autosomal recessive cutis laxa type 2 | (Orphanet:90350) |
| Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
| Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
| Autosomal recessive omodysplasia | (Orphanet:93329) |
| Autosomal recessive polycystic kidney disease | (Orphanet:731) |
| Autosomal recessive spondylocostal dysostosis | (Orphanet:2311) |
| BRESEK syndrome | (Orphanet:85284) |
| Beemer-Ertbruggen syndrome | (Orphanet:1237) |
| Bilateral renal agenesis | (Orphanet:1848) |
| Bird headed-dwarfism, Montreal type | (Orphanet:2617) |
| Blepharophimosis-intellectual deficit syndrome, Ohdo type | (Orphanet:2728) |
| Blepharophimosis-intellectual deficit syndrome, SBBYS type | (Orphanet:3047) |
| Bohring-Opitz syndrome | (Orphanet:97297) |
| Braddock syndrome | (Orphanet:52047) |
| Branchio-oculo-facial syndrome | (Orphanet:1297) |
| C syndrome | (Orphanet:1308) |
| CHARGE syndrome | (Orphanet:138) |
| Campomelic dysplasia | (Orphanet:140) |
| Camptodactyly syndrome, Guadalajara type 1 | (Orphanet:1327) |
| Cardiocranial syndrome, Pfeiffer type | (Orphanet:2872) |
| Cardiofaciocutaneous syndrome | (Orphanet:1340) |
| Cartilage-hair hypoplasia | (Orphanet:175) |
| Cataract - aberrant oral frenula - growth delay | (Orphanet:1373) |
| Cataract - intellectual deficit - hypogonadism | (Orphanet:1387) |
| Catel-Manzke syndrome | (Orphanet:1388) |
| Cerebro-facio-thoracic dysplasia | (Orphanet:1394) |
| Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
| Cerebro-reno-digital syndrome | (Orphanet:1396) |
| Chondrodysplasia, Blomstrand type | (Orphanet:50945) |
| Cleft palate - short stature - vertebral anomalies | (Orphanet:2015) |
| Cloverleaf skull - multiple congenital anomalies | (Orphanet:93267) |
| Conductive deafness - malformed external ear | (Orphanet:3216) |
| Congenital osteogenesis imperfecta - microcephaly - cataracts | (Orphanet:2772) |
| Cooper-Jabs syndrome | (Orphanet:1488) |
| Corneal-cerebellar syndrome | (Orphanet:3177) |
| Cornelia de Lange syndrome | (Orphanet:199) |
| Corpus callosum agenesis - double urinary collecting system | (Orphanet:1492) |
| Costello syndrome | (Orphanet:3071) |
| Crane-Heise syndrome | (Orphanet:1512) |
| Craniofacial dyssynostosis | (Orphanet:1516) |
| Craniomicromelic syndrome | (Orphanet:1524) |
| Craniosynostosis - fibular aplasia | (Orphanet:1533) |
| Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis | (Orphanet:171839) |
| Craniotelencephalic dysplasia | (Orphanet:1528) |
| Cutis laxa | (Orphanet:209) |
| Cyprus facial-neuromusculoskeletal syndrome | (Orphanet:2674) |
| Deafness - genital anomalies - metacarpal and metatarsal synostosis | (Orphanet:3224) |
| Deafness - intellectual deficit, Martin-Probst type | (Orphanet:85321) |
| Delayed speech - facial asymmetry - strabismus - ear lobe creases | (Orphanet:3038) |
| Desbuquois syndrome | (Orphanet:1425) |
| Desmosterolosis | (Orphanet:35107) |
| Diabetic embryopathy | (Orphanet:1926) |
| Diastrophic dwarfism | (Orphanet:628) |
| Disorder of sex development - intellectual deficit | (Orphanet:2983) |
| Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
| Distal limb deficiencies - micrognathia syndrome | (Orphanet:1307) |
| Distal monosomy 10p | (Orphanet:1580) |
| Distal monosomy 17q | (Orphanet:1597) |
| Distal monosomy 19p13.3 | (Orphanet:96129) |
| Distal monosomy 3p | (Orphanet:1620) |
| Distal monosomy 6p | (Orphanet:96125) |
| Distal monosomy 9p | (Orphanet:1642) |
| Distal trisomy 18q | (Orphanet:1716) |
| Distal trisomy 6p | (Orphanet:1745) |
| Donnai-Barrow syndrome | (Orphanet:2143) |
| Dubowitz syndrome | (Orphanet:235) |
| Dysmorphism - multiple structural anomalies | (Orphanet:1780) |
| Ear-patella-short stature syndrome | (Orphanet:2554) |
| Ectodermal dysplasia - intellectual deficit - central nervous system malformation | (Orphanet:1812) |
| Ectodermal dysplasia syndrome | (Orphanet:79373) |
| Edinburgh malformation syndrome | (Orphanet:1895) |
| Ehlers-Danlos syndrome, musculocontractural type | (Orphanet:2953) |
| Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
| Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria | (Orphanet:1035) |
| Endomyocardial fibroelastosis | (Orphanet:2022) |
| Eye defects - arachnodactyly - cardiopathy | (Orphanet:2725) |
| Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation | (Orphanet:1970) |
| Facial dysmorphism - shawl scrotum - joint laxity | (Orphanet:1778) |
| Familial visceral myopathy | (Orphanet:2604) |
| Femoral-facial syndrome | (Orphanet:1988) |
| Fetal Gaucher disease | (Orphanet:85212) |
| Fetal akinesia deformation sequence | (Orphanet:994) |
| Fetal alcohol syndrome | (Orphanet:1915) |
| Fetal hydantoin syndrome | (Orphanet:1912) |
| Fetal minoxidil syndrome | (Orphanet:1918) |
| Fetal trimethadione syndrome | (Orphanet:1913) |
| Fibrochondrogenesis | (Orphanet:2021) |
| Fine-Lubinsky syndrome | (Orphanet:1272) |
| Flat face - microstomia - ear anomaly | (Orphanet:1968) |
| Floating-Harbor syndrome | (Orphanet:2044) |
| Focal dermal hypoplasia | (Orphanet:2092) |
| Fraser syndrome | (Orphanet:2052) |
| Frontonasal dysplasia | (Orphanet:250) |
| Frontonasal dysplasia with alopecia and genital anomaly | (Orphanet:228390) |
| Fryns syndrome | (Orphanet:2059) |
| Fuhrmann syndrome | (Orphanet:2854) |
| GAPO syndrome | (Orphanet:2067) |
| GMS syndrome | (Orphanet:2090) |
| Genito-palato-cardiac syndrome | (Orphanet:2075) |
| Genitopatellar syndrome | (Orphanet:85201) |
| Goldenhar syndrome | (Orphanet:374) |
| Gonadal dysgenesis, XY type - associated anomalies | (Orphanet:1770) |
| Gómez-López-Hernández syndrome | (Orphanet:1532) |
| Hartsfield-Bixler-Demyer syndrome | (Orphanet:2117) |
| Hennekam syndrome | (Orphanet:2136) |
| Hepatic fibrosis - renal cysts - intellectual deficit | (Orphanet:2031) |
| Hereditary orotic aciduria | (Orphanet:30) |
| Hernandez-Aguirre Negrete syndrome | (Orphanet:2139) |
| Hirschsprung disease - nail hypoplasia - dysmorphism | (Orphanet:2153) |
| Holoprosencephaly - caudal dysgenesis | (Orphanet:2165) |
| Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
| Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
| Hydrocephalus - costovertebral dysplasia - Sprengel anomaly | (Orphanet:2180) |
| Hydrolethalus | (Orphanet:2189) |
| Hypertelorism - hypospadias - polysyndactyly syndrome | (Orphanet:2211) |
| Hypertelorism, Teebi type | (Orphanet:1519) |
| Hypomandibular faciocranial dysostosis | (Orphanet:1790) |
| Hypospadias - intellectual deficit, Goldblatt type | (Orphanet:2261) |
| ICF syndrome | (Orphanet:2268) |
| IMAGe syndrome | (Orphanet:85173) |
| Imperforate oropharynx - costo vetebral anomalies | (Orphanet:2759) |
| Intellectual deficit - hypotonia - skin hyperpigmentation | (Orphanet:3050) |
| Intellectual deficit, X-linked - dysmorphism - cerebral atrophy | (Orphanet:2958) |
| Intellectual deficit, X-linked - short stature - obesity | (Orphanet:3055) |
| Intellectual deficit, X-linked, Armfield type | (Orphanet:85276) |
| Intellectual deficit, X-linked, Wittwer type | (Orphanet:85291) |
| Isolated anterior cervical hypertrichosis | (Orphanet:3387) |
| Isolated cloverleaf skull syndrome | (Orphanet:2343) |
| Isotretinoin-like syndrome | (Orphanet:2306) |
| Jacobsen syndrome | (Orphanet:2308) |
| Joubert syndrome | (Orphanet:475) |
| Joubert syndrome with hepatic defect | (Orphanet:1454) |
| Joubert syndrome with ocular defect | (Orphanet:220493) |
| Joubert syndrome with oculorenal defect | (Orphanet:2318) |
| Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
| Joubert syndrome with renal defect | (Orphanet:220497) |
| KBG syndrome | (Orphanet:2332) |
| Kaler-Garrity-Stern syndrome | (Orphanet:2324) |
| Kapur-Toriello syndrome | (Orphanet:2328) |
| Kenny-Caffey syndrome | (Orphanet:2333) |
| Kousseff syndrome | (Orphanet:2351) |
| Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
| Langer-Giedion syndrome | (Orphanet:502) |
| Larsen-like osseous dysplasia - short stature | (Orphanet:2370) |
| Lateral meningocele syndrome | (Orphanet:2789) |
| Laurence-Moon syndrome | (Orphanet:2377) |
| Lethal Kniest-like dysplasia | (Orphanet:2347) |
| Lethal congenital contracture syndrome type 1 | (Orphanet:1486) |
| Lethal multiple pterygium syndrome | (Orphanet:33108) |
| Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
| Lethal restrictive dermopathy | (Orphanet:1662) |
| Leukocyte adhesion deficiency | (Orphanet:2968) |
| Lower limb deficiency - hypospadias | (Orphanet:2487) |
| Lowry-MacLean syndrome | (Orphanet:2409) |
| Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
| Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
| Marden-Walker syndrome | (Orphanet:2461) |
| Matthew-Wood syndrome | (Orphanet:2470) |
| McDonough syndrome | (Orphanet:2471) |
| Meckel syndrome | (Orphanet:564) |
| Mesomelic dwarfism - cleft palate - camptodactyly | (Orphanet:2631) |
| Metatropic dysplasia | (Orphanet:2635) |
| Mevalonic aciduria | (Orphanet:29) |
| Micro syndrome | (Orphanet:2510) |
| Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
| Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
| Microcephaly - brachydactyly - kyphoscoliosis | (Orphanet:3433) |
| Microcephaly - cervical spine fusion anomalies | (Orphanet:2522) |
| Microcephaly - deafness - intellectual deficit | (Orphanet:2533) |
| Microphthalmia, Lenz type | (Orphanet:568) |
| Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
| Monosomy 13q14 | (Orphanet:1587) |
| Monosomy 18p | (Orphanet:1598) |
| Monosomy 5p | (Orphanet:281) |
| Monosomy 9p | (Orphanet:261112) |
| Monosomy 9q22.3 | (Orphanet:77301) |
| Morse-Rawnsley-Sargent syndrome | (Orphanet:2570) |
| Mosaic trisomy 14 | (Orphanet:1703) |
| Mosaic trisomy 8 | (Orphanet:96061) |
| Mosaic trisomy 9 | (Orphanet:99776) |
| Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
| Mullerian derivatives - lymphangiectasia - polydactyly | (Orphanet:1655) |
| Multiple benign circumferential skin creases on limbs | (Orphanet:2505) |
| Multiple epiphyseal dysplasia, Al-Gazali type | (Orphanet:166024) |
| Nager syndrome | (Orphanet:245) |
| Neonatal adrenoleukodystrophy | (Orphanet:44) |
| Neurofaciodigitorenal syndrome | (Orphanet:2673) |
| Neurofibromatosis - Noonan syndrome | (Orphanet:638) |
| Night blindness - skeletal anomalies - dysmorphism | (Orphanet:1390) |
| Non-distal trisomy 10q | (Orphanet:1695) |
| Non-eruption of teeth - maxillary hypoplasia - genu valgum | (Orphanet:2972) |
| Non-rhizomelic chondrodysplasia punctata | (Orphanet:176) |
| Noonan syndrome | (Orphanet:648) |
| Noonan syndrome with multiple lentigines | (Orphanet:500) |
| Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
| Oculocerebrorenal syndrome | (Orphanet:534) |
| Okamoto syndrome | (Orphanet:2729) |
| Opitz G/BBB syndrome | (Orphanet:2745) |
| Orofaciodigital syndrome type 3 | (Orphanet:2752) |
| Orofaciodigital syndrome type 4 | (Orphanet:2753) |
| Osteocraniostenosis | (Orphanet:2763) |
| Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
| Otopalatodigital syndrome | (Orphanet:669) |
| PHAVER syndrome | (Orphanet:2876) |
| Pallister-Hall syndrome | (Orphanet:672) |
| Patterson-Stevenson-Fontaine syndrome | (Orphanet:2439) |
| Pelvis-shoulder dysplasia | (Orphanet:2839) |
| Pentasomy X | (Orphanet:11) |
| Perlman syndrome | (Orphanet:2849) |
| Peroxisomal acyl-CoA oxidase deficiency | (Orphanet:2971) |
| Peters-plus syndrome | (Orphanet:709) |
| Pfeiffer syndrome type 1 | (Orphanet:93258) |
| Pfeiffer syndrome type 2 | (Orphanet:93259) |
| Pfeiffer syndrome type 3 | (Orphanet:93260) |
| Pilotto syndrome | (Orphanet:2894) |
| Platyspondylic dysplasia, Torrance type | (Orphanet:85166) |
| Polysyndactyly - cardiac malformation | (Orphanet:2934) |
| Polyvalvular heart disease syndrome | (Orphanet:228410) |
| Postaxial acrofacial dysostosis | (Orphanet:246) |
| Progeroid syndrome, Petty type | (Orphanet:2963) |
| Prominent glabella - microcephaly - hypogenitalism | (Orphanet:2083) |
| Proteus syndrome | (Orphanet:744) |
| Pterygium colli - intellectual deficit - digital anomalies | (Orphanet:2988) |
| Ptosis - upper ocular movement limitation - absence of lacrimal punctum | (Orphanet:228396) |
| Pyknoachondrogenesis | (Orphanet:3003) |
| Recombinant 8 syndrome | (Orphanet:96167) |
| Renal-genital-middle ear anomalies | (Orphanet:1092) |
| Richieri Costa-Pereira syndrome | (Orphanet:3102) |
| Ring chromosome 10 | (Orphanet:1438) |
| Rubinstein-Taybi syndrome | (Orphanet:783) |
| SCARF syndrome | (Orphanet:3134) |
| Saethre-Chotzen syndrome | (Orphanet:794) |
| Sanjad-Sakati syndrome | (Orphanet:2323) |
| Say-Barber-Miller syndrome | (Orphanet:3132) |
| Schinzel-Giedion syndrome | (Orphanet:798) |
| Schwartz-Jampel syndrome | (Orphanet:800) |
| Short rib-polydactyly syndrome | (Orphanet:1505) |
| Short stature - craniofacial anomalies - genital hypoplasia | (Orphanet:2994) |
| Short stature - wormian bones - dextrocardia | (Orphanet:2863) |
| Shprintzen-Goldberg syndrome | (Orphanet:2462) |
| Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
| Smith-Lemli-Opitz syndrome | (Orphanet:818) |
| Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |
| Splenogonadal fusion - limb defects - micrognathia | (Orphanet:2063) |
| Split hand - urinary anomalies - spina bifida | (Orphanet:2437) |
| Spondylo-ocular syndrome | (Orphanet:85194) |
| Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
| Subaortic stenosis - short stature | (Orphanet:3191) |
| Summitt syndrome | (Orphanet:3210) |
| TARP syndrome | (Orphanet:2886) |
| Temtamy syndrome | (Orphanet:1777) |
| Tetrasomy 18p | (Orphanet:3307) |
| Thanatophoric dysplasia | (Orphanet:2655) |
| Thin ribs - tubular bones - dysmorphism | (Orphanet:1506) |
| Thrombocytopenia - Robin sequence | (Orphanet:3323) |
| Thrombocytopenia - absent radius | (Orphanet:3320) |
| Thymic-renal-anal-lung dysplasia | (Orphanet:3326) |
| Toluene embryopathy | (Orphanet:1920) |
| Toriello-Carey syndrome | (Orphanet:3338) |
| Trigonocephaly - short stature - developmental delay | (Orphanet:3369) |
| Triploidy | (Orphanet:3376) |
| Trisomy 12p | (Orphanet:1699) |
| Trisomy 13 | (Orphanet:3378) |
| Trisomy 17p | (Orphanet:261290) |
| Trisomy 18 | (Orphanet:3380) |
| Trisomy 1q | (Orphanet:261344) |
| Trisomy 20p | (Orphanet:261318) |
| Trisomy 4p | (Orphanet:1738) |
| Trisomy 8q | (Orphanet:1752) |
| VACTERL/VATER association | (Orphanet:887) |
| Verloove Vanhorick-Brubakk syndrome | (Orphanet:3429) |
| Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay | (Orphanet:73246) |
| Walker-Warburg syndrome | (Orphanet:899) |
| Weaver syndrome | (Orphanet:3447) |
| White forelock with malformations | (Orphanet:2475) |
| Williams syndrome | (Orphanet:904) |
| Wolf-Hirschhorn syndrome | (Orphanet:280) |
| X-linked dominant chondrodysplasia, Chassaing-Lacombe type | (Orphanet:163966) |
| X-linked intellectual deficit with marfanoid habitus | (Orphanet:776) |
| X-linked mandibulofacial dysostosis | (Orphanet:1131) |
| Yunis-Varon syndrome | (Orphanet:3472) |