Low-set, posteriorly rotated ears

Symptom Information:

Symptom ID: HPO:0000368
Synonyms:
Low-set posteriorly rotated ears [HPO:0000368]
Increased ear posterior angulation [Orphanet:13040]
Low set ear [Orphanet:13040]
Posteriorly rotated ear (disorder) [Orphanet:13040]
Low set ears (disorder) [Orphanet:13040]
Posteriorly rotated ear [Orphanet:13040]
Low set ears [Orphanet:13040]
Low-set posteriorly rotated ears [OMIM:Low-set posteriorly rotated ears]
Low-set, posteriorly rotated ears [OMIM:Low-set, posteriorly rotated ears]
Low set ears/posteriorly rotated ears [Orphanet:13040]
Low set ears [MedDRA:10024929]
Low-set ear [OMIM:Low-set ear]
Low-set ears (1 patient) [OMIM:Low-set ears (1 patient)]
Low-set ears (28%) [OMIM:Low-set ears (28%)]
Low-set ears (3 patients) [OMIM:Low-set ears (3 patients)]
Low-set ears (45%) [OMIM:Low-set ears (45%)]
Low-set ears (in 2/4 patients) [OMIM:Low-set ears (in 2/4 patients)]
Low-set ears (in one family) [OMIM:Low-set ears (in one family)]
Low-set ears (in some patients) [OMIM:Low-set ears (in some patients)]
Low-set ears (severe form) [OMIM:Low-set ears (severe form)]
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:0000358 "Posteriorly rotated ears" [Orphanet:13040]
HPO:0000369 "Low-set ears" [Orphanet:13040]
Orphanet:13040 "Low set ears/posteriorly rotated ears" [Orphanet:13040]
OMIM: "Low-set posteriorly rotated ears" [OMIM:Low-set posteriorly rotated ears]
OMIM: "Low-set, posteriorly rotated ears" [OMIM:Low-set, posteriorly rotated ears]
OMIM: "Low-set ear" [OMIM:Low-set ear]
OMIM: "Low-set ears (1 patient)" [OMIM:Low-set ears (1 patient)]
OMIM: "Low-set ears (28%)" [OMIM:Low-set ears (28%)]
OMIM: "Low-set ears (3 patients)" [OMIM:Low-set ears (3 patients)]
OMIM: "Low-set ears (45%)" [OMIM:Low-set ears (45%)]
OMIM: "Low-set ears (in 2/4 patients)" [OMIM:Low-set ears (in 2/4 patients)]
OMIM: "Low-set ears (in one family)" [OMIM:Low-set ears (in one family)]
OMIM: "Low-set ears (in some patients)" [OMIM:Low-set ears (in some patients)]
OMIM: "Low-set ears (severe form)" [OMIM:Low-set ears (severe form)]
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]
UMLS:C0239234 "Low set ears" [Orphanet:13040]
Is a (Direct Parents):
MedDRA External ear disorders congenital
Orphanet Posteriorly rotated ears
HPO         Posteriorly rotated ears
HPO         Low-set ears
Orphanet Abnormality of the outer ear
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)
                   Low-set, posteriorly rotated ears(HPO:0000368)
                Low-set ears(HPO:0000369)
                   Low-set, posteriorly rotated ears(HPO:0000368)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Ear and labyrinthine disorders congenital(MedDRA:10013995)
       External ear disorders congenital(MedDRA:10015733)
          Low-set, posteriorly rotated ears(HPO:0000368)
Database Frequency: 38 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
2p21 microdeletion syndrome (Orphanet:163693)
3q13 microdeletion syndrome (Orphanet:1621)
5p13 microduplication syndrome (Orphanet:329802)
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES (OMIM:300887)
AREDYLD syndrome (Orphanet:1133)
Atypical hypotonia - cystinuria syndrome (Orphanet:238523)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant multiple pterygium syndrome (Orphanet:65743)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Baller-Gerold syndrome (Orphanet:1225)
Bardet-Biedl syndrome (Orphanet:110)
CEREBROOCULOFACIOSKELETAL SYNDROME 4 (OMIM:610758)
COG1-CDG (Orphanet:263508)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
FACIAL PARESIS, HEREDITARY CONGENITAL, 3 (OMIM:614744)
Frontonasal dysplasia (Orphanet:250)
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome (Orphanet:306542)
Hereditary sensory and autonomic neuropathy type 6 (Orphanet:314381)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hypotonia - cystinuria syndrome (Orphanet:163690)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Legius syndrome (Orphanet:137605)
Leprechaunism (Orphanet:508)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 12 (OMIM:614562)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 (OMIM:614114)
Mowat-Wilson syndrome (Orphanet:2152)
NEMALINE MYOPATHY 2 (OMIM:256030)
NOONAN SYNDROME 1 (OMIM:163950)
NOONAN SYNDROME 4 (OMIM:610733)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis (Orphanet:65288)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)