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Browse result for Rett syndrome

※ introduction

    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.

Reference
DiseaseOntology: Rett syndrome



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD01650P516084204
MECP2
Methyl-CpG-binding protein 2
Homo sapiens
PTMD05641P553162290
FOXG1
Forkhead box protein G1
Homo sapiens
PTMD01960Q9Z2D617257
Mecp2
Methyl-CpG-binding protein 2
Mus musculus