Disease association ontology term - MONDO:0975826 - arthrogryposis multiplex congenita 7, X-linked

Term summary

ID: MONDO:0975826
Name: arthrogryposis multiplex congenita 7, X-linked
Ontology or CV name: Disease association

Parents

is_a arthrogryposis multiplex congenita

Annotation

Disease association

MONDO:0975826 - arthrogryposis multiplex congenita 7, X-linked

References:

PB_REF:0000006

Genes:

tho2 (SPAC1D4.14)