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Disease association ontology term - MONDO:0020504 - hereditary recurrent myoglobinuria

Term summary

ID
MONDO:0020504
Name
hereditary recurrent myoglobinuria
Ontology or CV name
Disease association
Definition
An inborn error of metabolism characterized by abnormal urinary excretion of myoglobin due to acute destruction of skeletal muscle fibers.

Parents

Annotation

Disease association

MONDO:0009992 - myoglobinuria, acute recurrent, autosomal recessive

References:

Genes: