Prolidase deficiency (Q40028): Difference between revisions
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Changed label, description and/or aliases in pt-br, en |
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| description / pt-br | description / pt-br | ||
A deficiência de prolidase é um erro inato do metabolismo muito raro, caracterizado por lesões cutâneas leves a graves, particularmente na face, palmas das mãos, pernas e plantas dos pés, juntamente com outras características variáveis. | |||
| description / en | description / en | ||
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. | |||
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. |
