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Human Disease

autosomal recessive intellectual developmental disorder 9/26

Term ID
DOID:0081184
Synonyms
Definition
An autosomal recessive intellectual developmental disorder that has_material_basis_in linkage to a 9.1-Mb region on proximal chromosome 14q between SNPs rs10132585 and rs1278951, termed the MRT9 locus. https://pubmed.ncbi.nlm.nih.gov/21629298/
References
Ontology
Human Disease   ( DOID:0081184 )
Relationships
is a type of
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Genes Involved
Zebrafish Models