Disease association ontology term - MONDO:0013472 - fatal infantile hypertonic myofibrillar myopathy
Term summary
ID
MONDO:0013472
Name
fatal infantile hypertonic myofibrillar myopathy
Ontology or CV name
Disease association
Parents
is_a
myofibrillar myopathy
Annotation
Disease association
MONDO:0013472
-
fatal infantile hypertonic myofibrillar myopathy
References:
PB_REF:0000006
Genes:
hsp16 (SPBC3E7.02c)
hsp20 (SPCC338.06c)