Abnormally folded helix

Symptom Information:

Symptom ID: HPO:0008544
Synonyms:
Abnormally folded helix [OMIM:Abnormally folded helix]
Quality:
Cross references:
OMIM: "Abnormally folded helix" [OMIM:Abnormally folded helix]
Is a (Direct Parents):
HPO         Abnormality of the helix
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:
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)