DISEASES

Disease-gene associations mined from literature

Human genes for Ogden syndrome

Ogden syndrome [DOID:0050781]

A syndrome characterized by postnatal growth failure, severely delayed psychomotor development, variable dysmorphic features, and hypotonia and has_material_basis_in X-linked recessive or X-linked dominant mutation in the NAA10 gene on chromosome Xq28.

Synonyms:  Ogden syndrome,  DOID:0050781,  Ogden disease,  Ogden disorder,  Ogden syndromes ...

Linkouts:  OMIM #1 #2