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Human Disease

neurodevelopmental disorder with spasticity and poor growth

Term ID
DOID:0070421
Synonyms
  • 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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models