Prolidase deficiency (Q40028): Difference between revisions
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Latest revision as of 05:40, 13 August 2026
Prolidase deficiency is a very rare inborn error of metabolism characterised by mild to severe skin lesions particularly on the face, palms, lower legs and soles, together with other variable features.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C50.F0 |
||
| English | Prolidase deficiency |
Prolidase deficiency is a very rare inborn error of metabolism characterised by mild to severe skin lesions particularly on the face, palms, lower legs and soles, together with other variable features. |
Statements
CID11:5C50.F0
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dki-india-5C50.F0
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Concluído
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13 August 2026
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