Posteriorly rotated ears

Symptom Information:

Symptom ID: HPO:0000358
Synonyms:
Ear, posterior angulation, increased [HPO:0000358]
Posteriorly angulated ears [HPO:0000358]
Posteriorly rotated [HPO:0000358]
Posteriorly rotated auricles [HPO:0000358]
Posteriorly-angulated ears [HPO:0000358]
Posteriorly-rotated ears [HPO:0000358]
Increased ear posterior angulation [Orphanet:13040]
Posteriorly rotated ear [HPO:0000358]
Posteriorly rotated ear (disorder) [Orphanet:13040]
Posteriorly rotated ear [Orphanet:13040]
Posteriorly angulated ears [OMIM:Posteriorly angulated ears]
Posteriorly rotated auricles [OMIM:Posteriorly rotated auricles]
Posteriorly rotated ears [OMIM:Posteriorly rotated ears]
Posteriorly-angulated ears [OMIM:Posteriorly-angulated ears]
Posteriorly-rotated ears [OMIM:Posteriorly-rotated ears]
Low set ears/posteriorly rotated ears [Orphanet:13040]
Posteriorly rotated ears (1/4 patients) [OMIM:Posteriorly rotated ears (1/4 patients)]
Posteriorly rotated ears (2p21del) [OMIM:Posteriorly rotated ears (2p21del)]
Posteriorly rotated ears (female) [OMIM:Posteriorly rotated ears (female)]
Posteriorly rotated ears (in some patients) [OMIM:Posteriorly rotated ears (in some patients)]
Quality:
Cross references:
HPO:0000368 "Low-set, posteriorly rotated ears" [Orphanet:13040]
Orphanet:13040 "Low set ears/posteriorly rotated ears" [Orphanet:13040]
OMIM: "Posteriorly angulated ears" [OMIM:Posteriorly angulated ears]
OMIM: "Posteriorly rotated auricles" [OMIM:Posteriorly rotated auricles]
OMIM: "Posteriorly rotated ears" [OMIM:Posteriorly rotated ears]
OMIM: "Posteriorly-angulated ears" [OMIM:Posteriorly-angulated ears]
OMIM: "Posteriorly-rotated ears" [OMIM:Posteriorly-rotated ears]
OMIM: "Posteriorly rotated ears (1/4 patients)" [OMIM:Posteriorly rotated ears (1/4 patients)]
OMIM: "Posteriorly rotated ears (2p21del)" [OMIM:Posteriorly rotated ears (2p21del)]
OMIM: "Posteriorly rotated ears (female)" [OMIM:Posteriorly rotated ears (female)]
OMIM: "Posteriorly rotated ears (in some patients)" [OMIM:Posteriorly rotated ears (in some patients)]
UMLS:C0431478 "Posteriorly rotated ear" [Orphanet:13040]
Is a (Direct Parents):
Orphanet Abnormality of the outer ear
HPO         Abnormal location of ears
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)
                Posteriorly rotated ears(HPO:0000358)
MedDRA:
Database Frequency: 163 / 7739
Resource:

All diseases associated with this symptom:

16p11.2p12.2 microdeletion syndrome (Orphanet:261211)
1p36 deletion syndrome (Orphanet:1606)
2p21 microdeletion syndrome (Orphanet:163693)
3q29 microdeletion syndrome (Orphanet:65286)
8q22.1 microdeletion syndrome (Orphanet:178303)
AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA (OMIM:613623)
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES (OMIM:300887)
AREDYLD syndrome (Orphanet:1133)
AURICULOCONDYLAR SYNDROME 1 (OMIM:602483)
AURICULOCONDYLAR SYNDROME 2 (OMIM:614669)
Acro-renal-mandibular syndrome (Orphanet:958)
Acrocallosal syndrome (Orphanet:36)
Acrofacial dysostosis, Rodriguez type (Orphanet:1788)
Alpha-thalassemia - X-linked intellectual deficit syndrome (Orphanet:847)
Atypical hypotonia - cystinuria syndrome (Orphanet:238523)
Auriculocondylar syndrome (Orphanet:137888)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive facio-digito-genital syndrome (Orphanet:1974)
Bardet-Biedl syndrome (Orphanet:110)
Bohring-Opitz syndrome (Orphanet:97297)
Braddock syndrome (Orphanet:52047)
Branchio-oculo-facial syndrome (Orphanet:1297)
C syndrome (Orphanet:1308)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CARDIOFACIOCUTANEOUS SYNDROME 2 (OMIM:615278)
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION (OMIM:601088)
CEREBROOCULOFACIOSKELETAL SYNDROME 4 (OMIM:610758)
CHROMOSOME 16q22 DELETION SYNDROME (OMIM:614541)
CHROMOSOME 5q12 DELETION SYNDROME (OMIM:615668)
CK syndrome (Orphanet:251383)
CREE MENTAL RETARDATION SYNDROME (OMIM:606851)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Carpenter-Waziri syndrome (Orphanet:93973)
Cataract - aberrant oral frenula - growth delay (Orphanet:1373)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Costello syndrome (Orphanet:3071)
DIAMOND-BLACKFAN ANEMIA 10 (OMIM:613309)
Desmosterolosis (Orphanet:35107)
Distal monosomy 6p (Orphanet:96125)
Donnai-Barrow syndrome (Orphanet:2143)
Dysmorphism - conductive hearing loss - heart defect (Orphanet:289553)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
Ehlers-Danlos syndrome, musculocontractural type (Orphanet:2953)
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS (OMIM:227255)
FACIAL PARESIS, HEREDITARY CONGENITAL, 3 (OMIM:614744)
FEINGOLD SYNDROME 1 (OMIM:164280)
FRONTOOCULAR SYNDROME (OMIM:605321)
Fabry disease (Orphanet:324)
Feingold syndrome (Orphanet:1305)
Fetal Gaucher disease (Orphanet:85212)
Fetal akinesia deformation sequence (Orphanet:994)
Fine-Lubinsky syndrome (Orphanet:1272)
Floating-Harbor syndrome (Orphanet:2044)
Gorlin-Chaudhry-Moss syndrome (Orphanet:2095)
Growth deficiency - brachydactyly - dysmorphism (Orphanet:2055)
Gómez-López-Hernández syndrome (Orphanet:1532)
HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION (OMIM:613870)
HYPERTELORISM AND TETRALOGY OF FALLOT (OMIM:239711)
HYPERTRICHOSIS, HYPERKERATOSIS, MENTAL RETARDATION, AND DISTINCTIVEFACIAL FEATURES (OMIM:609943)
Hartsfield-Bixler-Demyer syndrome (Orphanet:2117)
Hermansky-Pudlak syndrome with neutropenia (Orphanet:183678)
Holmes-Gang syndrome (Orphanet:93970)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Hyperphosphatasia-intellectual deficiency syndrome (Orphanet:247262)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Hypotonia - cystinuria syndrome (Orphanet:163690)
Hypotonia with lactic acidemia and hyperammonemia (Orphanet:137908)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Intellectual deficit, X-linked, Brooks type (Orphanet:3056)
Intellectual deficit, X-linked, Kroes type (Orphanet:163961)
Joubert syndrome 14 (OMIM:614424)
Joubert syndrome with orofaciodigital defect (Orphanet:2754)
Juberg-Marsidi syndrome (Orphanet:93972)
KABUKI SYNDROME 1 (OMIM:147920)
Kabuki syndrome (Orphanet:2322)
LEOPARD SYNDROME 1 (OMIM:151100)
LEOPARD SYNDROME 3 (OMIM:613707)
Lateral meningocele syndrome (Orphanet:2789)
Leprechaunism (Orphanet:508)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY (OMIM:606369)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 (OMIM:615866)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 32 (OMIM:616268)
MGAT2-CDG (Orphanet:79329)
MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLARATROPHY (OMIM:615760)
MICROPHTHALMIA WITH CYST, BILATERAL FACIAL CLEFTS, AND LIMB ANOMALIES (OMIM:607597)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
Mandibulofacial dysostosis - macroblepharon - macrostomia (Orphanet:357158)
Mevalonic aciduria (Orphanet:29)
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type (Orphanet:217026)
Microcornea-myopic chorioretinal atrophy-telecanthus syndrome (Orphanet:369970)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Microphthalmia with limb anomalies (Orphanet:1106)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Miller-Dieker syndrome (Orphanet:531)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Monosomy 9p (Orphanet:261112)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mowat-Wilson syndrome (Orphanet:2152)
Multiple epiphyseal dysplasia, Lowry type (Orphanet:166016)
Nager syndrome (Orphanet:245)
Non-eruption of teeth - maxillary hypoplasia - genu valgum (Orphanet:2972)
Noonan syndrome with multiple lentigines (Orphanet:500)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
OROFACIODIGITAL SYNDROME VI (OMIM:277170)
OTOFACIOOSSEOUS-GONADAL SYNDROME (OMIM:601976)
Oculofaciocardiodental syndrome (Orphanet:2712)
Ondine syndrome (Orphanet:661)
Opitz G/BBB syndrome (Orphanet:2745)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Otopalatodigital syndrome (Orphanet:669)
Otopalatodigital syndrome type 2 (Orphanet:90652)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
POLYCYSTIC KIDNEY DISEASE, POTTER TYPE I, WITH MICROBRACHYCEPHALY,HYPERTELORISM, AND BRACHYMELIA (OMIM:263210)
PYCR1-related DeBarsy syndrome (Orphanet:293633)
Pachygyria - epilepsy - intellectual deficit - dysmorphism (Orphanet:94084)
Pallister-Hall syndrome (Orphanet:672)
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Orphanet:65288)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Prominent glabella - microcephaly - hypogenitalism (Orphanet:2083)
Pseudoaminopterin syndrome (Orphanet:221120)
Pterygium colli - intellectual deficit - digital anomalies (Orphanet:2988)
ROBERTS SYNDROME (OMIM:268300)
Recombinant 8 syndrome (Orphanet:96167)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Roberts syndrome (Orphanet:3103)
SC PHOCOMELIA SYNDROME (OMIM:269000)
SCARF syndrome (Orphanet:3134)
SENER SYNDROME (OMIM:606156)
SIMOSA CRANIOFACIAL SYNDROME (OMIM:182150)
STEVENSON-CAREY SYNDROME (OMIM:611961)
Sanjad-Sakati syndrome (Orphanet:2323)
Schilbach-Rott syndrome (Orphanet:2353)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Simpson-Golabi-Behmel syndrome type 2 (Orphanet:79022)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Spondylo-ocular syndrome (Orphanet:85194)
Spondyloepimetaphyseal dysplasia, aggrecan type (Orphanet:171866)
Spondylometaphyseal dysplasia, Sedaghatian type (Orphanet:93317)
Syndromic multisystem autoimmune disease due to Itch deficiency (Orphanet:228426)
TARP syndrome (Orphanet:2886)
TEMPLE SYNDROME (OMIM:616222)
TMEM165-CDG (Orphanet:314667)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME (OMIM:300280)
Velo-facial-skeletal syndrome (Orphanet:3424)
WIDOW'S PEAK SYNDROME (OMIM:314570)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
Zellweger syndrome (Orphanet:912)
Zimmermann-Laband syndrome (Orphanet:3473)
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME (OMIM:601321)