Disease-gene associations mined from literature

Human genes for Rett syndrome

Rett syndrome [DOID:1206]

A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability.

Synonyms:  Rett syndrome,  DOID:1206,  Rett disease,  Rett disorder,  Rett's disorder ...

Linkouts:  OMIM #1 #2