Large earlobe
Symptom Information:
Symptom ID: | HPO:0009748 | ||||||||
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) Abnormality of earlobe(HPO:0000363) Large earlobe(HPO:0009748) MedDRA: |
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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) |