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Summary Literature (0)
DOID:0080044 - hypochondrogenesis

Disease Ontology Definition:An osteochondrodysplasia that has_material_basis_in a mutation in the COL2A1 gene which affects bone growth and results_in a small body, hydrops fetalis, and abnormal ossification located_in vertebral column or located_in pelvis. The disease has_symptom enlarged abdomen.

Synonyms:

Xenbase Genes : col2a1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019669 - hypochondrogenesis


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): monogenic disease (is_a), osteochondrodysplasia (is_a), spinal disease (is_a)