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