Summary Literature (0)

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

Echinobase Genes : LOC577399, taf2, med23, pgap1, mettl23, kptn, tti2, nsun2


MIM:

MIM:249500 - mental retardation, autosomal recessive 1; mrt1

MIM:607417 - mental retardation, autosomal recessive 2; mrt2

MIM:608443 - mental retardation, autosomal recessive 3; mrt3

MIM:611091 - mental retardation, autosomal recessive 5; mrt5

MIM:611092 - mental retardation, autosomal recessive 6; mrt6

MIM:611093 - mental retardation, autosomal recessive 7; mrt7

MIM:614020 - mental retardation, autosomal recessive 14; mrt14

MIM:614249 - mental retardation, autosomal recessive 18; mrt18

MIM:614340 - mental retardation, autosomal recessive 27; mrt27

MIM:614499 - mental retardation, autosomal recessive 34; mrt34

MIM:615493 - mental retardation, autosomal recessive 37; mrt37

MIM:615541 - mental retardation, autosomal recessive 39; mrt39

MIM:615599 - mental retardation, autosomal recessive 40; mrt40

MIM:615637 - mental retardation, autosomal recessive 41; mrt41

MIM:615802 - mental retardation, autosomal recessive 42; mrt42

MIM:615817 - mental retardation, autosomal recessive 43; mrt43

MIM:615942 - mental retardation, autosomal recessive 44; mrt44

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee