Protruding ear
Symptom Information:
Symptom ID: | HPO:0000411 | ||||||||||
Synonyms: |
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Quality: | |||||||||||
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) Protruding ear(HPO:0000411) MedDRA: |
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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) |