Search Ontology:
Human Disease

Ferguson-Bonni neurodevelopmental syndrome

Term ID
DOID:0070677
Synonyms
Definition
A syndromic intellectual disability characterized by global developmental delay, impaired intellectual development, and hypotonia with early motor delay that has_material_basis_in homozygous mutation in the ANAPC7 gene on chromosome 12q24. https://pmc.ncbi.nlm.nih.gov/articles/PMC8741739/
References
Ontology
Human Disease   ( DOID:0070677 )
Relationships
Other Pages
Genes Involved
Zebrafish Models
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