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DO Term : fibrochondrogenesis 2 [DOID:0080673] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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

synonyms:
OMIM:614524,
614524

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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