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DOID:0060308 - autosomal recessive intellectual developmental disorder
Disease Ontology Definition:A intellectual disability characterized by an autosomal recessive inheritance pattern.
Synonyms: autosomal recessive mental retardation, autosomal recessive non-syndromic mental retardation,
Xenbase Genes : tnik, ezr, tbcd, kptn, tusc3, kdm5b, camk2a, lingo1, st3gal3, pgap3, dcps, pigc, fbxo31, ndst1, slc45a1,
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive disease (is_a),
intellectual disability (is_a),
non-syndromic intellectual disability (is_a)