Human genes for hypochondroplasia
Hypochondroplasia [DOID:0080041]
An osteochondrodysplasia that has_material_basis_in mutation in the FGFR3 gene which affects ossification of cartilage and results_in short limb dwarfism.
Synonyms: hypochondroplasia, DOID:0080041, hypochondroplasias
Linkouts: OMIM