Hereditary methemoglobinemia

Orpha code: 621OMIM code: 250800

Definition

A rare red cell disorder classified principally into two clinical phenotypes: autosomal recessive congenital (or hereditary) methemoglobinemia types I and II (RCM/RHM type 1; RCM/RHM type 2).

Disease data
Classification

Disease

Synonyms
Autosomal recessive methemoglobinemia
Methemoglobinemia wrodzona
Autosomalna recesywna methemoglobinemia
Congenital methemoglobinemia
ORPHA code
621
OMIM code
250800
ICD10 code
D74.0
ICD11 code
3A92

No additional description.

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