Abnormal location of ears

Symptom Information:

Symptom ID: HPO:0000357
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the outer ear
HPO         Anteverted ears
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the ear(HPO:0000598)
          Abnormality of the outer ear(HPO:0000356)
             Abnormal location of ears(HPO:0000357)
Database Frequency: 328 / 7739

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)