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Human Disease

autosomal dominant intellectual developmental disorder 62

Term ID
DOID:0061035
Synonyms
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in caused by heterozygous mutation in the DLG4 gene on chromosome 17p13. https://pubmed.ncbi.nlm.nih.gov/29460436/
References
Ontology
Human Disease   ( DOID:0061035 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models