Hypoplasia of the ear cartilage
Symptom Information:
Symptom ID: | HPO:0100720 | ||||
Synonyms: |
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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) Hypoplasia of the ear cartilage(HPO:0100720) MedDRA: |
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Database Frequency: | 12 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive polycystic kidney disease | (Orphanet:731) |
Bazex-Dupré-Christol syndrome | (Orphanet:113) |
C syndrome | (Orphanet:1308) |
CHARGE syndrome | (Orphanet:138) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria | (Orphanet:1035) |
Galloway-Mowat syndrome | (Orphanet:2065) |
Intellectual deficit - athetosis - microphthalmia | (Orphanet:1236) |
Prader-Willi syndrome | (Orphanet:739) |
Teebi-Shaltout syndrome | (Orphanet:3291) |
Tetraploidy | (Orphanet:3305) |
Thymic-renal-anal-lung dysplasia | (Orphanet:3326) |