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Human Disease

autosomal recessive intellectual developmental disorder 30

Term ID
DOID:0081195
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in linkage to a 22-Mb region on proximal chromosome 6q between SNPs rs4612125 and rs285651. https://pubmed.ncbi.nlm.nih.gov/21629298/
References
Ontology
Human Disease   ( DOID:0081195 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models