ACROMIAL DIMPLES
General Information (adopted from Orphanet):
| Synonyms, Signs: |
SUPRASPINOUS FOSSAE, CONGENITAL |
| Number of Symptoms | 3 |
| OrphanetNr: | |
| OMIM Id: |
102350
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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:0000951) | Abnormality of the skin | 147 / 7739 | ||||
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(OMIM) | Acromial dimples | 3 / 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:
| Description: (OMIM) |
Acromial dimples are skin depressions overlying the acromial process of the scapula. They are thought to arise from the entrapment of tissue between a bony structure and the uterine wall. The skin and bone become compressed and tethering ... |
| Clinical Description OMIM |
Beillard et al. (2005) described 7 individuals with bi-acromial dimples without associated malformation. In 5 of the 7, the diagnosis was fortuitous, suggesting that these dimples represent a common and likely underdiagnosed condition. Although the dimples are thought ... |