Cupped ear
Symptom Information:
Symptom ID: | HPO:0000378 | ||||||||||
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) Abnormality of the pinna(HPO:0000377) Cupped ear(HPO:0000378) MedDRA: |
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Database Frequency: | 34 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
15q24 microdeletion syndrome | (Orphanet:94065) |
2q23.1 microdeletion syndrome | (Orphanet:228402) |
Agenesis of the corpus callosum - intellectual deficit - coloboma - micrognathia | (Orphanet:52055) |
Atrioventricular defect - blepharophimosis -radial defects | (Orphanet:1352) |
Auriculocondylar syndrome | (Orphanet:137888) |
Autosomal dominant nonsyndromic intellectual deficit | (Orphanet:178469) |
BOR syndrome | (Orphanet:107) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
BRANCHIOOTIC SYNDROME 1 | (OMIM:602588) |
BRANCHIOOTORENAL SYNDROME 1 | (OMIM:113650) |
Bartsocas-Papas syndrome | (Orphanet:1234) |
Blepharophimosis - epicanthus inversus - ptosis | (Orphanet:126) |
CHARGE syndrome | (Orphanet:138) |
Desmosterolosis | (Orphanet:35107) |
Fraser syndrome | (Orphanet:2052) |
Growth deficiency - brachydactyly - dysmorphism | (Orphanet:2055) |
HIRSCHSPRUNG DISEASE, CARDIAC DEFECTS, AND AUTONOMIC DYSFUNCTION | (OMIM:613870) |
Intellectual deficit, X-linked, Brooks type | (Orphanet:3056) |
KABUKI SYNDROME 2 | (OMIM:300867) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
MENTAL RETARDATION, X-LINKED 93 | (OMIM:300659) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Microcephaly - deafness - intellectual deficit | (Orphanet:2533) |
Mowat-Wilson syndrome | (Orphanet:2152) |
OTOFACIOCERVICAL SYNDROME 2 | (OMIM:615560) |
Pfeiffer-Palm-Teller syndrome | (Orphanet:2871) |
Pitt-Hopkins syndrome | (Orphanet:2896) |
Postaxial acrofacial dysostosis | (Orphanet:246) |
Renpenning syndrome | (Orphanet:3242) |
SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS | (OMIM:609654) |
SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1 | (OMIM:119100) |
Scalp-ear-nipple syndrome | (Orphanet:2036) |
Tibial aplasia - ectrodactyly | (Orphanet:3329) |
Warsaw breakage syndrome | (Orphanet:280558) |