Search Ontology:
Human Disease
neurodevelopmental disorder with spasticity and poor growth
- Term ID
- DOID:0070421
- Synonyms
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- NEDSG
- Definition
- An autosomal recessive intellectual developmental disorder characterized by axial hypotonia, delayed psychomotor development, poor feeding, and failure to thrive with onset in early infancy that has_material_basis_in homozygous mutation in the UFC1 gene on chromosome 1q23. https://pubmed.ncbi.nlm.nih.gov/29868776/
- References
- Ontology
- Human Disease ( DOID:0070421 )
- is a type of
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Genes Involved
Zebrafish Models