Defects of catalase and peroxidase

Preferred Label : Defects of catalase and peroxidase;

Inclusion CIM-10 : Acatalasia [Takahara];

Rare : true;

Diag associé à un acte (%) : 100.0;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

E803;

UMLS CUI

C0494349;

Automatic exact mappings (from CISMeF team)
- Inborn errors of porphyrin or heme metabolism [ICD-11 Category]
Orphanet concepts
- Acatalasemia [ORDO Disease]
- Disorder of porphyrin and heme metabolism [ORDO Disease]
- Myeloperoxidase deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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