wikipathways-collection

WikiPathways WP4808

Summary

Fails

InteractionTests.interactionsWithLabels

Interactions found that involve Labels: 18

http://classic.wikipathways.org/instance/WP4808_r128905 "Hypertrophy" with graphId b7a
http://classic.wikipathways.org/instance/WP4808_r128905 "WNT signaling
canonical / non-canonical" with graphId bed
http://classic.wikipathways.org/instance/WP4808_r128905 "Proliferation" with graphId d5f
http://classic.wikipathways.org/instance/WP4808_r128905 "BMPs" with graphId b2d
http://classic.wikipathways.org/instance/WP4808_r128905 "Mineralization" with graphId e4d
http://classic.wikipathways.org/instance/WP4808_r128905 "Dying" with graphId b59
http://classic.wikipathways.org/instance/WP4808_r128905 "Full differentiation" with graphId fba0c
http://classic.wikipathways.org/instance/WP4808_r128905 "Integrins" with graphId d3b0f
http://classic.wikipathways.org/instance/WP4808_r128905 "Vascular invasion" with graphId e31d0
http://classic.wikipathways.org/instance/WP4808_r128905 "Gs" with graphId fc068
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:600430
Chromosome 2q37 deletion syndrome" with graphId f8e71
http://classic.wikipathways.org/instance/WP4808_r128905 "Osteoblastic
differentiation" with graphId f20
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:613073
Metaphyseal anadysplasia 2" with graphId e6bf2
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:156500
Metaphyseal chondrodysplasia, Schmid type" with graphId f4641
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:245150
Keutel syndrome" with graphId c0def
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:614732
Intrauterine growth retardation, metaphyseal dysplasia, 
adrenal hypoplasia congenita, and genital anomalies" with graphId f99f8
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:271665
Spondylometaepiphyseal dysplasia, short limb-hand type" with graphId b7cc5
http://classic.wikipathways.org/instance/WP4808_r128905 "OMIM:613848
Osteogenesis imperfecta, type X" with graphId aa6b4