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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
Reference
DiseaseOntology: Rett syndrome
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD01650 | P51608 | 4204 | MECP2 | Methyl-CpG-binding protein 2 | Homo sapiens |
| PTMD05641 | P55316 | 2290 | FOXG1 | Forkhead box protein G1 | Homo sapiens |
| PTMD01960 | Q9Z2D6 | 17257 | Mecp2 | Methyl-CpG-binding protein 2 | Mus musculus |
