Search Ontology:
Human Disease

autosomal recessive intellectual developmental disorder 60

Term ID
DOID:0081222
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the TAF13 gene on chromosome 1p13. https://pubmed.ncbi.nlm.nih.gov/28257693/
References
Ontology
Human Disease   ( DOID:0081222 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models