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neurodevelopmental disorder with or without seizures and gait abnormalities
Disease Summary
Associated Targets (1)
Tclin
1
Uniprot Description An autosomal dominant neurodevelopmental disorder characterized by global developmental delay apparent from infancy or early childhood, mild to profound intellectual disability, hypertonia early in life, which progresses to spasticity and impaired gait later, and behavioral abnormalities. Some patients may develop seizures of variable severity early in life.
Mondo Term and Equivalent IDs
MONDO:0060641: neurodevelopmental disorder with or without seizures and gait abnormalities
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:617864
UMLS:CN800195
MONDO:0060641
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