Overfolded helix

Symptom Information:

Symptom ID: HPO:0000396
Synonyms:
Over-folded helices [HPO:0000396]
Overfolded ears [HPO:0000396]
Overfolded helices [HPO:0000396]
Over-folded helices [OMIM:Over-folded helices]
Overfolded ears [OMIM:Overfolded ears]
Overfolded helices [OMIM:Overfolded helices]
Overfolded helix [OMIM:Overfolded helix]
Folded helix [Orphanet:13200]
Folded helices [OMIM:Folded helices]
Folded helix [OMIM:Folded helix]
Quality:
Cross references:
Orphanet:13200 "Folded helix" [Orphanet:13200]
OMIM: "Over-folded helices" [OMIM:Over-folded helices]
OMIM: "Overfolded ears" [OMIM:Overfolded ears]
OMIM: "Overfolded helices" [OMIM:Overfolded helices]
OMIM: "Overfolded helix" [OMIM:Overfolded helix]
OMIM: "Folded helices" [OMIM:Folded helices]
OMIM: "Folded helix" [OMIM:Folded helix]
Is a (Direct Parents):
HPO         Abnormally folded 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)
                   Abnormally folded helix(HPO:0008544)
                      Overfolded helix(HPO:0000396)
MedDRA:
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

BARAITSER-WINTER SYNDROME 1 (OMIM:243310)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Baraitser-Winter syndrome (Orphanet:2995)
Branchio-oculo-facial syndrome (Orphanet:1297)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Congenital contractural arachnodactyly (Orphanet:115)
Down syndrome (Orphanet:870)
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES (OMIM:614684)
Hypertelorism - hypospadias - polysyndactyly syndrome (Orphanet:2211)
Koolen-De Vries syndrome (Orphanet:96169)
MICROPHTHALMIA, SYNDROMIC 1 (OMIM:309800)
MIDFACE HYPOPLASIA, OBESITY, DEVELOPMENTAL DELAY, AND NEONATAL HYPOTONIA (OMIM:608624)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Marshall-Smith syndrome (Orphanet:561)
Multiple congenital anomalies - hypotonia - seizures syndrome (Orphanet:280633)
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (Orphanet:300496)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Prominent glabella - microcephaly - hypogenitalism (Orphanet:2083)
SHORT STATURE AND FACIOAURICULOTHORACIC MALFORMATIONS (OMIM:609654)
Schwartz-Jampel syndrome (Orphanet:800)
Zunich-Kaye syndrome (Orphanet:3474)