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Human Disease

autosomal recessive intellectual developmental disorder 31

Term ID
DOID:0081191
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in linkage to a 10.5-Mb region on proximal chromosome 4q between SNPs rs11944876 and rs6551838. https://pubmed.ncbi.nlm.nih.gov/21063731/
References
Ontology
Human Disease   ( DOID:0081191 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models