Term Name: fibrochondrogenesis 2
Synonyms:
Definition: A fibrochondrogenesis that has_material_basis_in homozygous or heterozygous mutation in the COL11A2 gene on chromosome 6p21.3.
Ontology: Human Disease [DOID:0080673]   ( DOID:0080673 )

Relationships
is a type of: autosomal dominant disease autosomal recessive disease fibrochondrogenesis