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neurodevelopmental disorder with involuntary movements
Summary
- Synonym
-
- NEDIM
- Definition
- A movement disease characterized by delayed psychomotor development and infantile or childhood onset of hyperkinetic involuntary movements, including chorea and athetosis that has_material_basis_in heterozygous mutation of the GNAO1 gene on chromosome 16q13.
- Super Class
- autosomal dominant disease movement disease
External Links
- Disease Ontology
- DOID:0112276
- Mondo Disease Ontology
- OMIM
- MGI genotype (from TogoID)
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0009381 | Short finger |
| HP:0010174 | Broad phalanx of the toes |
| HP:0010818 | Generalized tonic seizure |
| HP:0010819 | Atonic seizure |
| HP:0010850 | EEG with spike-wave complexes |
| HP:0010851 | EEG with burst suppression |
| HP:0011169 | Generalized clonic seizure |
| HP:0011190 | Uni- and bilateral multifocal epileptiform discharges |
| HP:0012448 | Delayed myelination |
| HP:0012469 | Infantile spasms |
