Genetic syndromes with poikiloderma (Q44243): Difference between revisions
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Latest revision as of 11:38, 13 August 2026
Hereditary syndromes in which poikiloderma (cutaneous pigmentation, atrophy and telangiectasia) is a conspicuous feature.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | EC10 |
||
| English | Genetic syndromes with poikiloderma |
Hereditary syndromes in which poikiloderma (cutaneous pigmentation, atrophy and telangiectasia) is a conspicuous feature. |
Statements
CID11:EC10
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dki-india-EC10
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Concluído
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13 August 2026
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