Abnormality of the helix

Symptom Information:

Symptom ID: HPO:0011039
Synonyms:
Abnormal helices [HPO:0011039]
Helix abnormal [HPO:0011039]
Abnormal helices [OMIM:Abnormal helices]
Helix abnormal [OMIM:Helix abnormal]
Quality:
Cross references:
OMIM: "Abnormal helices" [OMIM:Abnormal helices]
OMIM: "Helix abnormal" [OMIM:Helix abnormal]
Is a (Direct Parents):
HPO         Abnormality of the pinna
HPO         Squared superior portion of 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)
MedDRA:
Database Frequency: 33 / 7739
Resource:

All diseases associated with this symptom:

ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 (OMIM:170995)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Alpha-mannosidosis (Orphanet:61)
Beckwith-Wiedemann syndrome (Orphanet:116)
Blepharoptosis - myopia - ectopia lentis (Orphanet:1259)
CHARGE syndrome (Orphanet:138)
CODAS syndrome (Orphanet:1458)
Cerebro-reno-digital syndrome (Orphanet:1396)
Congenital contractural arachnodactyly (Orphanet:115)
Distal monosomy 9p (Orphanet:1642)
Endomyocardial fibroelastosis (Orphanet:2022)
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation (Orphanet:1970)
Fetal trimethadione syndrome (Orphanet:1913)
Fryns syndrome (Orphanet:2059)
Hypertelorism, Teebi type (Orphanet:1519)
Lamellar ichthyosis (Orphanet:313)
Lethal Kniest-like dysplasia (Orphanet:2347)
Lung agenesis - heart defect - thumb anomalies (Orphanet:1120)
Mikati-Najjar-Sahli syndrome (Orphanet:2558)
Neurofibromatosis - Noonan syndrome (Orphanet:638)
Noonan syndrome (Orphanet:648)
Norrie disease (Orphanet:649)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Orofaciodigital syndrome type 4 (Orphanet:2753)
Osteocraniostenosis (Orphanet:2763)
Oto-onycho-peroneal syndrome (Orphanet:2793)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) (OMIM:214110)
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) (OMIM:614866)
Saethre-Chotzen syndrome (Orphanet:794)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Trisomy 13 (Orphanet:3378)
Zellweger syndrome (Orphanet:912)