Cupped ear

Symptom Information:

Symptom ID: HPO:0000378
Synonyms:
Capuchin ears [HPO:0000378]
Cup-shaped ears [HPO:0000378]
CUPPED EARS [HPO:0000378]
Simple, cup-shaped ears [HPO:0000378]
Cup-shaped ears [OMIM:Cup-shaped ears]
Cupped ears [OMIM:Cupped ears]
Simple, cup-shaped ears [OMIM:Simple, cup-shaped ears]
Cup-shaped ears (30-60% of patients) [OMIM:Cup-shaped ears (30-60% of patients)]
Cupped ears (in some patients) [OMIM:Cupped ears (in some patients)]
Simple cup-shaped ears [OMIM:Simple cup-shaped ears]
Quality:
Cross references:
OMIM: "Cup-shaped ears" [OMIM:Cup-shaped ears]
OMIM: "Cupped ears" [OMIM:Cupped ears]
OMIM: "Simple, cup-shaped ears" [OMIM:Simple, cup-shaped ears]
OMIM: "Cup-shaped ears (30-60% of patients)" [OMIM:Cup-shaped ears (30-60% of patients)]
OMIM: "Cupped ears (in some patients)" [OMIM:Cupped ears (in some patients)]
OMIM: "Simple cup-shaped ears" [OMIM:Simple cup-shaped ears]
Is a (Direct Parents):
HPO         Abnormality of the pinna
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:
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)