ICD-11 classes
14 Diseases of the skin
Genetic and developmental disorders affecting the skin
Genetic disorders of amino acid metabolism or transport...
5C50.F0 — Prolidase deficiency
ICD-11 5C50.F0 — 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.
The diagnosis includes nothing.
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere: