Protruding ear

Symptom Information:

Symptom ID: HPO:0000411
Synonyms:
Prominent ear [HPO:0000411]
Protruding ears [HPO:0000411]
Prominent ear (disorder) [Orphanet:13060]
Prominent ear [Orphanet:13060]
Protruding ears [OMIM:Protruding ears]
Prominent/bat ears [Orphanet:13060]
Prominent ears (in some patients) [OMIM:Prominent ears (in some patients)]
Prominent ears (rare) [OMIM:Prominent ears (rare)]
Protruding ears (in some patients) [OMIM:Protruding ears (in some patients)]
Protruding ears (rare) [OMIM:Protruding ears (rare)]
Quality:
Cross references:
HPO:0000412 "Prominent ears" [Orphanet:13060]
HPO:0009904 "Prominent ear helix" [Orphanet:13060]
Orphanet:13060 "Prominent/bat ears" [Orphanet:13060]
OMIM: "Protruding ears" [OMIM:Protruding ears]
OMIM: "Prominent ears (in some patients)" [OMIM:Prominent ears (in some patients)]
OMIM: "Prominent ears (rare)" [OMIM:Prominent ears (rare)]
OMIM: "Protruding ears (in some patients)" [OMIM:Protruding ears (in some patients)]
OMIM: "Protruding ears (rare)" [OMIM:Protruding ears (rare)]
UMLS:C1305420 "Prominent ear" [Orphanet:13060]
Is a (Direct Parents):
Orphanet Abnormality of the outer ear
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)
                Protruding ear(HPO:0000411)
MedDRA:
Database Frequency: 140 / 7739
Resource:

All diseases associated with this symptom:

14q12 microdeletion syndrome (Orphanet:261144)
15q13.3 microdeletion syndrome (Orphanet:199318)
16p13.3 microduplication syndrome (Orphanet:96078)
16q24.3 microdeletion syndrome (Orphanet:261250)
17q12 microdeletion syndrome (Orphanet:261265)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
3M syndrome (Orphanet:2616)
8q21.11 microdeletion syndrome (Orphanet:284160)
ADAMS-OLIVER SYNDROME 2 (OMIM:614219)
Abruzzo-Erickson syndrome (Orphanet:921)
Aicardi syndrome (Orphanet:50)
Alagille syndrome (Orphanet:52)
Allan-Herndon-Dudley syndrome (Orphanet:59)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Autosomal dominant microcephaly (Orphanet:2514)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
Autosomal recessive chorioretinopathy-microcephaly (Orphanet:2518)
Autosomal recessive cutis laxa type 2B (Orphanet:357064)
BRESEK syndrome (Orphanet:85284)
Barth syndrome (Orphanet:111)
Bloom syndrome (Orphanet:125)
CARPENTER SYNDROME 2 (OMIM:614976)
COLD-INDUCED SWEATING SYNDROME 2 (OMIM:610313)
Caudal appendage - deafness (Orphanet:1123)
Cenani-Lenz syndrome (Orphanet:3258)
Char syndrome (Orphanet:46627)
Choanal atresia - deafness - cardiac defects - dysmorphism (Orphanet:1200)
Cleft palate - large ears - small head (Orphanet:2013)
Coffin-Lowry syndrome (Orphanet:192)
Congenital muscular dystrophy, Ullrich type (Orphanet:75840)
Congenital unilateral hypoplasia of depressor anguli oris (Orphanet:1166)
Cranioectodermal dysplasia 4 (OMIM:614378)
Deafness - genital anomalies - metacarpal and metatarsal synostosis (Orphanet:3224)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Distal 22q11.2 microduplication syndrome (Orphanet:261337)
Distal monosomy 10q (Orphanet:96148)
Dubowitz syndrome (Orphanet:235)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 2 (OMIM:615539)
Ectodermal dysplasia - blindness (Orphanet:1806)
Ehlers-Danlos syndrome, musculocontractural type (Orphanet:2953)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Erythrokeratodermia variabilis (Orphanet:317)
Facial dysmorphism - shawl scrotum - joint laxity (Orphanet:1778)
Faciocardiorenal syndrome (Orphanet:1973)
Familial lambdoid synostosis (Orphanet:3267)
Fibulo-ulnar hypoplasia - renal anomalies (Orphanet:2256)
Fragile X syndrome (Orphanet:908)
Frank-Ter Haar syndrome (Orphanet:137834)
GAPO syndrome (Orphanet:2067)
GRANDDAD SYNDROME (OMIM:138920)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Harrod syndrome (Orphanet:2115)
Hepatic fibrosis - renal cysts - intellectual deficit (Orphanet:2031)
Hidrotic ectodermal dysplasia, Halal type (Orphanet:1809)
Hydrocephalus - blue sclerae - nephropathy (Orphanet:2186)
Intellectual deficit - hypoplastic corpus callosum - preauricular tag (Orphanet:1495)
Intellectual deficit - myopathy - short stature - endocrine defect (Orphanet:3068)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Intellectual deficit, X-linked - hypogammaglobulinemia - progressive neurological deterioration (Orphanet:85317)
Intellectual deficit, X-linked - hypotonia - facial dysmorphism - aggressive behavior (Orphanet:85329)
Intellectual deficit, X-linked, Abidi type (Orphanet:85273)
Intellectual deficit, X-linked, Brooks type (Orphanet:3056)
Intellectual deficit, X-linked, Pai type (Orphanet:85322)
Intellectual deficit, X-linked, Raymond type (Orphanet:163953)
KABUKI SYNDROME 2 (OMIM:300867)
Kabuki syndrome (Orphanet:2322)
Koolen-De Vries syndrome (Orphanet:96169)
LEOPARD SYNDROME 1 (OMIM:151100)
Langer-Giedion syndrome (Orphanet:502)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
MELAS (Orphanet:550)
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE (OMIM:300861)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
McDonough syndrome (Orphanet:2471)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Micrencephaly - corpus callosum agenesis - abnormal genitalia (Orphanet:2508)
Microcephaly - deafness - intellectual deficit (Orphanet:2533)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Microphthalmia with brain and digit anomalies (Orphanet:139471)
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies (Orphanet:369897)
Monosomy 13q14 (Orphanet:1587)
Monosomy 18p (Orphanet:1598)
Monosomy 22q13 (Orphanet:48652)
Mosaic trisomy 8 (Orphanet:96061)
Nance-Horan syndrome (Orphanet:627)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Noonan syndrome with multiple lentigines (Orphanet:500)
Norrie disease (Orphanet:649)
OSTEOGENESIS IMPERFECTA, TYPE XIII (OMIM:614856)
OTOFACIOOSSEOUS-GONADAL SYNDROME (OMIM:601976)
Occipital horn syndrome (Orphanet:198)
Oculocerebrorenal syndrome (Orphanet:534)
Odontotrichomelic syndrome (Orphanet:2723)
Okamoto syndrome (Orphanet:2729)
Osteoglophonic dwarfism (Orphanet:2645)
Otodental syndrome (Orphanet:2791)
Otofaciocervical syndrome (Orphanet:2792)
PROGEROID FACIAL APPEARANCE WITH HAND ANOMALIES (OMIM:602249)
PTERYGIUM COLLI, ISOLATED (OMIM:177990)
Peters-plus syndrome (Orphanet:709)
Pfeiffer-Palm-Teller syndrome (Orphanet:2871)
Phocomelia, Schinzel type (Orphanet:2879)
Preaxial polydactyly - colobomata - intellectual deficit (Orphanet:2921)
Pseudoprogeria syndrome (Orphanet:2985)
Pterygium colli - intellectual deficit - digital anomalies (Orphanet:2988)
Radio-ulnar synostosis - intellectual deficit - hypotonia (Orphanet:3270)
Renpenning syndrome (Orphanet:3242)
Richieri Costa-Pereira syndrome (Orphanet:3102)
SCHIZOPHRENIA 1 (OMIM:181510)
Say-Barber-Miller syndrome (Orphanet:3132)
Scalp-ear-nipple syndrome (Orphanet:2036)
Schilbach-Rott syndrome (Orphanet:2353)
Schinzel-Giedion syndrome (Orphanet:798)
Sheldon-Hall syndrome (Orphanet:1147)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Syndromic X-linked intellectual deficit due to JARID1C mutation (Orphanet:85279)
THREE M SYNDROME 2 (OMIM:612921)
THREE M SYNDROME 3 (OMIM:614205)
TRICHORHINOPHALANGEAL SYNDROME, TYPE III (OMIM:190351)
TRICHORRHEXIS NODOSA SYNDROME (OMIM:275550)
Thumb deformity - alopecia - pigmentation anomaly (Orphanet:2251)
Toluene embryopathy (Orphanet:1920)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Trisomy 20p (Orphanet:261318)
Trisomy 5p (Orphanet:1742)
Trisomy 8q (Orphanet:1752)
Trisomy 9p (Orphanet:236)
Van den Ende-Gupta syndrome (Orphanet:2460)
Visceral neuropathy - brain anomalies - facial dysmorphism - developmental delay (Orphanet:73246)
Walker-Warburg syndrome (Orphanet:899)
Weaver-Williams syndrome (Orphanet:3448)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Williams syndrome (Orphanet:904)
Woodhouse-Sakati syndrome (Orphanet:3464)
Woolly hair - hypotrichosis - everted lower lip - outstanding ears (Orphanet:1409)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
X-linked mandibulofacial dysostosis (Orphanet:1131)
Zlotogora-Ogur syndrome (Orphanet:3253)