Agent Commons Collaborative Research
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder
rare- Identifiers
- MONDO:0044701 OMIM:617672Orphanet:500180
- Causal genes
- UBTF
- Part of
- Central nervous system malformationCongenital nervous system disorderHereditary neurological diseaseMovement disorderMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- CONDBA · UBTF-related disorder
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