Prominent ear helix

Symptom Information:

Symptom ID: HPO:0009904
Synonyms:
Protruding ear [Orphanet:13060]
Prominent ear (disorder) [Orphanet:13060]
Prominent ear [Orphanet:13060]
Prominent/bat ears [Orphanet:13060]
Prominent ears (in some patients) [OMIM:Prominent ears (in some patients)]
Prominent ears (rare) [OMIM:Prominent ears (rare)]
Protruding ears (in some patients) [OMIM:Protruding ears (in some patients)]
Protruding ears (rare) [OMIM:Protruding ears (rare)]
Quality:
Cross references:
HPO:0000412 "Prominent ears" [Orphanet:13060]
HPO:0000411 "Protruding ear" [Orphanet:13060]
Orphanet:13060 "Prominent/bat ears" [Orphanet:13060]
OMIM: "Prominent ears (in some patients)" [OMIM:Prominent ears (in some patients)]
OMIM: "Prominent ears (rare)" [OMIM:Prominent ears (rare)]
OMIM: "Protruding ears (in some patients)" [OMIM:Protruding ears (in some patients)]
OMIM: "Protruding ears (rare)" [OMIM:Protruding ears (rare)]
UMLS:C1305420 "Prominent ear" [Orphanet:13060]
Is a (Direct Parents):
HPO         Abnormality of the helix
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 the helix(HPO:0011039)
                   Prominent ear helix(HPO:0009904)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

ADAMS-OLIVER SYNDROME 2 (OMIM:614219)
Bloom syndrome (Orphanet:125)
CARPENTER SYNDROME 2 (OMIM:614976)
Cranioectodermal dysplasia 4 (OMIM:614378)
Lethal osteosclerotic bone dysplasia (Orphanet:1832)
MELAS (Orphanet:550)
OSTEOGENESIS IMPERFECTA, TYPE XIII (OMIM:614856)
Woodhouse-Sakati syndrome (Orphanet:3464)