Posteriorly rotated ears
Symptom Information:
Symptom ID: | HPO:0000358 | ||||||||||||||||||||
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) Posteriorly rotated ears(HPO:0000358) MedDRA: |
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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) |