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Human Disease

autosomal recessive intellectual developmental disorder 23

Term ID
DOID:0081196
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in linkage to a 45.6-Mb interval in the pericentromeric region of chromosome 11 between SNPs rs604518 and rs10899421. https://pubmed.ncbi.nlm.nih.gov/21629298/
References
Ontology
Human Disease   ( DOID:0081196 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models