DISEASES

Disease-gene associations mined from literature

Human genes for trichodontoosseous syndrome

Trichodontoosseous syndrome [DOID:0111565]

A syndrome characterized by curly kinky hair at birth, enamel hypoplasia, taurodontism, thickening of cortical bones and variable expression of craniofacial morphology that has_material_basis_in heterozygous mutation in DLX3 on chromosome 17q21.33.

Synonyms:  trichodontoosseous syndrome,  DOID:0111565,  trichodontoosseous disease,  trichodontoosseous disorder,  trichodontoosseous syndromes ...