DISEASES

Disease-gene associations mined from literature

Human genes for hypochondroplasia

Hypochondroplasia [DOID:0080041]

An acromesomelic dysplasia that has_material_basis_in mutation in AMDH gene which results_in normal axial skeleton but fused bones in the located_in hand or located_in foot.

Synonyms:  hypochondroplasia,  DOID:0080041

Linkouts:  OMIM