Disease association ontology term - MONDO:0009992 - myoglobinuria, acute recurrent, autosomal recessive

Term summary

ID: MONDO:0009992
Name: myoglobinuria, acute recurrent, autosomal recessive
Ontology or CV name: Disease association

Parents

is_a hereditary recurrent myoglobinuria
is_a acute disease

Annotation

Disease association

MONDO:0009992 - myoglobinuria, acute recurrent, autosomal recessive

References:

PB_REF:0000006

Genes:

ned1 (SPAC1952.13)