Search Ontology:
Human Disease

autosomal recessive intellectual developmental disorder 40

Term ID
DOID:0081205
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the TAF2 gene on chromosome 8q24. https://pubmed.ncbi.nlm.nih.gov/34474177/
References
Ontology
Human Disease   ( DOID:0081205 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models