Large earlobe

Symptom Information:

Symptom ID: HPO:0009748
Synonyms:
Fleshy earlobes [HPO:0009748]
Prominent ear lobes [HPO:0009748]
prominent ear lobules [HPO:0009748]
Fleshy earlobes [OMIM:Fleshy earlobes]
Prominent ear lobes [OMIM:Prominent ear lobes]
Prominent ear lobules [OMIM:Prominent ear lobules]
Thick/wide ear lobe [Orphanet:13340]
Prominent ear lobule [OMIM:Prominent ear lobule]
Quality:
Cross references:
Orphanet:13340 "Thick/wide ear lobe" [Orphanet:13340]
OMIM: "Fleshy earlobes" [OMIM:Fleshy earlobes]
OMIM: "Prominent ear lobes" [OMIM:Prominent ear lobes]
OMIM: "Prominent ear lobules" [OMIM:Prominent ear lobules]
OMIM: "Prominent ear lobule" [OMIM:Prominent ear lobule]
Is a (Direct Parents):
HPO         Abnormality of earlobe
Orphanet Abnormality of the outer ear
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)
                Abnormality of earlobe(HPO:0000363)
                   Large earlobe(HPO:0009748)
MedDRA:
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

AARSKOG-SCOTT SYNDROME (OMIM:305400)
Borjeson-Forssman-Lehmann syndrome (Orphanet:127)
Costello syndrome (Orphanet:3071)
Cystic fibrosis - gastritis - megaloblastic anemia (Orphanet:2575)
Desmosterolosis (Orphanet:35107)
Diastrophic dwarfism (Orphanet:628)
Fabry disease (Orphanet:324)
Familial osteodysplasia, Anderson type (Orphanet:2769)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Hurler syndrome (Orphanet:93473)
Intellectual deficit - athetosis - microphthalmia (Orphanet:1236)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Maxillo-nasal dysplasia (Orphanet:1248)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Monosomy 9q22.3 (Orphanet:77301)
Mosaic trisomy 8 (Orphanet:96061)
Mowat-Wilson syndrome (Orphanet:2152)
Mucopolysaccharidosis type 2 (Orphanet:580)
Neurofaciodigitorenal syndrome (Orphanet:2673)
OCULODENTODIGITAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:257850)
Oculo-reno-cerebellar syndrome (Orphanet:2715)
Ring chromosome 10 (Orphanet:1438)
STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES (OMIM:612948)
Thickened earlobes - conductive deafness (Orphanet:2405)
Williams syndrome (Orphanet:904)
Wilson-Turner syndrome (Orphanet:3459)
Zimmermann-Laband syndrome (Orphanet:3473)