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Summary Literature (0)
DOID:0080673 - fibrochondrogenesis 2


Disease Ontology Definition:A fibrochondrogenesis that has_material_basis_in homozygous or heterozygous mutation in the COL11A2 gene on chromosome 6p21.3.

Synonyms:

Xenbase Genes : col11a2


OMIM:
OMIM:614524 - FIBROCHONDROGENESIS 2; FBCG2

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), autosomal recessive disease (is_a), fibrochondrogenesis (is_a)