Disease association ontology term - MONDO:0032751 - arthrogryposis, distal, type 2B3
Term summary
ID
MONDO:0032751
Name
arthrogryposis, distal, type 2B3
Ontology or CV name
Disease association
Parents
is_a
autosomal dominant disease
is_a
Sheldon-hall syndrome
Annotation
Disease association
MONDO:0032751
-
arthrogryposis, distal, type 2B3
References:
PB_REF:0000006
Genes:
myo2 (SPCC645.05c)
myp2 (SPAC4A8.05c)