fibrochondrogenesis 2

Term ID

DOID:0080673

Synonyms

Definition

A fibrochondrogenesis that has_material_basis_in homozygous or heterozygous mutation in the COL11A2 gene on chromosome 6p21.3. https://pubmed.ncbi.nlm.nih.gov/22246659/

References

OMIM:614524

Ontology

Human Disease ( DOID:0080673 )

Relationships

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

autosomal dominant disease autosomal recessive disease fibrochondrogenesis Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models

Citations