Abnormality of the helix
Symptom Information:
Symptom ID: | HPO:0011039 | ||||
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) MedDRA: |
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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) |