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Human Disease

neurodevelopmental disorder with hypotonia and speech delay

Term ID
DOID:0070512
Synonyms
  • NEDHSS
Definition
A syndrome characterized by global developmental delay, impaired intellectual development with poor or absent speech, and fine and gross motor delay that has_material_basis_in heterozygous or compound heterozygous mutation in the EIF4A2 gene on chromosome 3q27.3. https://pubmed.ncbi.nlm.nih.gov/36528028/
References
Ontology
Human Disease   ( DOID:0070512 )
Relationships
is a type of
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Genes Involved
Zebrafish Models