Angioma serpiginosum
General Information (adopted from Orphanet):
| Synonyms, Signs: |
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| Number of Symptoms | 13 |
| OrphanetNr: | 95429 |
| OMIM Id: |
106050
300652 |
| ICD-10: |
L81.7 |
| 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 X-linked recessive Not applicable [Orphanet] |
| Age of onset: |
Childhood [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Genetic skin vascular disease
-Rare genetic disease Skin vascular disease -Rare skin disease Vascular tumor -Rare circulatory system disease -Rare developmental defect during embryogenesis |
Symptom Information:
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(HPO:0008046) | Abnormality of the retinal vasculature | Occasional [Orphanet] | 41 / 7739 | |||
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(HPO:0000951) | Abnormality of the skin | Very frequent [Orphanet] | 147 / 7739 | |||
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(HPO:0011276) | Vascular skin abnormality | Very frequent [Orphanet] | 24 / 7739 | |||
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(HPO:0100585) | Telangiectasia of the skin | Very frequent [Orphanet] | 66 / 7739 | |||
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(HPO:0010783) | Erythema | Very frequent [Orphanet] | 138 / 7739 | |||
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(HPO:0000962) | Hyperkeratosis | 216 / 7739 | ||||
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(HPO:0001052) | Nevus flammeus | Very frequent [Orphanet] | 88 / 7739 | |||
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(HPO:0003677) | Slow progression | 134 / 7739 | ||||
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(MedDRA:10025421) | Macule | Very frequent [Orphanet] | 55 / 7739 | |||
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(HPO:0003621) | Juvenile onset | 105 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 | ||||
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(HPO:0012740) | Papilloma | Occasional [Orphanet] | 17 / 7739 | |||
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(HPO:0003745) | Sporadic | 131 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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