PATELLA, FAMILIAL RECURRENT DISLOCATION OF
General Information (adopted from Orphanet):
Synonyms, Signs: |
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Number of Symptoms | 3 |
OrphanetNr: | |
OMIM Id: |
169000
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ICD-10: |
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UMLs: |
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MeSH: |
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MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
Autosomal dominant inheritance [Omim] |
Age of onset: |
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Disease classification (adopted from Orphanet):
Parent Diseases: | No data available. |
Symptom Information:
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(HPO:0005001) | Recurrent patellar dislocation | 4 / 7739 | ||||
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(OMIM) | No joint laxity | 1 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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Additional Information:
Clinical Description OMIM |
Miller (1978) observed 12 persons with recurrent dislocation of the patella in 3 generations of a family with no male-to-male transmission. Six of those affected had genu valgum. Miller (1978) noted that Carter and Sweetnam (1960) had reported ... |