Search Ontology:
Human Disease

autosomal recessive intellectual developmental disorder 35

Term ID
DOID:0081201
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in linkage to a 12.2-Mb region on chromosome 17q21.31-q22 between SNPs rs4792947 and rs11079258. https://pubmed.ncbi.nlm.nih.gov/20950399/
References
Ontology
Human Disease   ( DOID:0081201 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models