DISEASES

Disease-gene associations mined from literature

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