Low-set, posteriorly rotated ears
Symptom Information:
Symptom ID: | HPO:0000368 | ||||||||||||||||||||||||
Synonyms: |
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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) 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) |
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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) |