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childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal dominant neurodegenerative disease with onset in childhood, characterized by progressive cortical atrophy, developmental delay, developmental regression, loss of motor skills and ambulation, absence of language, and intellectual disability.
Mondo Term and Equivalent IDs
MONDO:0044701:  childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
Orphanet:500180: 
UMLS:CN469330: