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Summary Literature (0)
DOID:0060308 - autosomal recessive non-syndromic intellectual disability


Disease Ontology Definition:A non-syndromic intellectual disability characterized by an autosomal recessive inheritance pattern.

Synonyms: autosomal recessive mental retardation, autosomal recessive non-syndromic mental retardation

In OMIM:
OMIM:249500 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 1; MRT1
OMIM:607417 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 2; MRT2
OMIM:608443 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 3; MRT3
OMIM:611091 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5; MRT5
OMIM:611092 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 6; MRT6
OMIM:611093 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 7; MRT7
OMIM:614020 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 14; MRT14
OMIM:614249 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 18; MRT18
OMIM:614340 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 27; MRT27
OMIM:614499 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 34, WITH VARIANT LISSENCEPHALY; MRT34
OMIM:615493 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 37; MRT37
OMIM:615541 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 39; MRT39
OMIM:615599 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 40; MRT40
OMIM:615637 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41; MRT41
OMIM:615802 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 42; MRT42
OMIM:615817 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 43; MRT43
OMIM:615942 - MENTAL RETARDATION, AUTOSOMAL RECESSIVE 44; MRT44

In Mondo Disease Ontology:
MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : tnik, ezr, kptn, tusc3, kdm5b, st3gal3, dcps, pigc, fbxo31, ndst1, slc45a1, lins1, aimp1, wars2, nsun2, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): non-syndromic intellectual disability (is_a)