Human genes for Crouzon syndrome-acanthosis nigricans syndrome
Crouzon syndrome-acanthosis nigricans syndrome [DOID:0111161]
A syndrome characterized by Crouzon-like features, premature synostosis of cranial sutures, and acanthosis nigricans that has_material_basis_in heterozygous missense mutation in the FGFR3 gene on chromosome 4p16.
Synonyms: Crouzon syndrome-acanthosis nigricans syndrome, Crouzon syndromeacanthosis nigricans syndrome, Crouzon syndrome-acanthosis nigricans disease, Crouzon syndrome-acanthosis nigricans disorder, Crouzon syndrome-acanthosis nigricans syndromes ...