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Human Disease

autosomal recessive intellectual developmental disorder 33

Term ID
DOID:0081194
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in linkage to chromosome 17p in an interval spanning 5.1 Mb between SNPs rs1367950 and rs1826925. https://pubmed.ncbi.nlm.nih.gov/21063731/
References
Ontology
Human Disease   ( DOID:0081194 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models