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autosomal recessive non-syndromic intellectual disability (DOID:0060308)
Synonyms: autosomal recessive mental retardation; autosomal recessive non-syndromic mental retardation
Alt IDs: OMIM:249500, OMIM:607417, OMIM:608443, OMIM:611090, OMIM:611091, OMIM:611092, OMIM:611093, OMIM:611095, OMIM:611096, OMIM:611097, OMIM:611107, OMIM:614020, OMIM:614208, OMIM:614249, OMIM:614329, OMIM:614333, OMIM:614340, OMIM:614341, OMIM:614342, OMIM:614343, OMIM:614344, OMIM:614345, OMIM:614346, OMIM:614347, OMIM:614499, OMIM:615493, OMIM:615516, OMIM:615541, OMIM:615599, OMIM:615637, OMIM:615802, OMIM:615817, OMIM:615942, ORDO:88616
Definition: A non-syndromic intellectual disability characterized by an autosomal recessive inheritance pattern.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/14/2017
MGI 6.08
The Jackson Laboratory