Abnormally folded helix
Symptom Information:
Symptom ID: | HPO:0008544 | ||
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 the helix(HPO:0011039) Abnormally folded helix(HPO:0008544) MedDRA: |
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Database Frequency: | 24 / 7739 | ||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
6p22 microdeletion syndrome | (Orphanet:251046) |
Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
Braddock syndrome | (Orphanet:52047) |
Branchiogenic deafness syndrome | (Orphanet:50815) |
CHARGE syndrome | (Orphanet:138) |
CODAS syndrome | (Orphanet:1458) |
Conductive deafness - malformed external ear | (Orphanet:3216) |
Diastrophic dwarfism | (Orphanet:628) |
Fetal trimethadione syndrome | (Orphanet:1913) |
Hypospadias - intellectual deficit, Goldblatt type | (Orphanet:2261) |
Imperforate oropharynx - costo vetebral anomalies | (Orphanet:2759) |
Isotretinoin-like syndrome | (Orphanet:2306) |
Koolen-De Vries syndrome | (Orphanet:96169) |
LUJAN-FRYNS SYNDROME | (OMIM:309520) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
Mesomelic dwarfism - cleft palate - camptodactyly | (Orphanet:2631) |
PHAVER syndrome | (Orphanet:2876) |
Prominent glabella - microcephaly - hypogenitalism | (Orphanet:2083) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Tibial aplasia - ectrodactyly | (Orphanet:3329) |
Urban-Rogers-Meyer syndrome | (Orphanet:3409) |