Disease association ontology term - MONDO:0017351 - inborn disorder of lysine and hydroxylysine metabolism
Term summary
ID
MONDO:0017351
Name
inborn disorder of lysine and hydroxylysine metabolism
Ontology or CV name
Disease association
Parents
is_a
inborn disorder of amino acid and other organic acid metabolism
is_a
inborn disorder of aspartate family metabolism
Annotation
Disease association
MONDO:0009388
-
hyperlysinemia
References:
PB_REF:0000006
Genes:
lys3 (SPAC227.18)
lys9 (SPBC3B8.03)