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Disease Ontology Browser
non-syndromic X-linked intellectual disability (DOID:0050776)
Synonyms: non-specific X-linked mental retardation
Alt IDs: OMIM:300046, OMIM:300047, OMIM:300062, OMIM:300114, OMIM:300115, OMIM:300143, OMIM:300210, OMIM:300271, OMIM:300324, OMIM:300355, OMIM:300372, OMIM:300387, OMIM:300428, OMIM:300433, OMIM:300436, OMIM:300454, OMIM:300498, OMIM:300504, OMIM:300505, OMIM:300518, OMIM:300558, OMIM:300577, OMIM:300659, OMIM:300716, OMIM:300802, OMIM:300803, OMIM:300844, OMIM:300848, OMIM:300849, OMIM:300850, OMIM:300851, OMIM:300852, OMIM:300912, OMIM:300919, OMIM:300923, OMIM:309530, OMIM:309549, ORDO:777
Definition: A non-syndromic intellectual disability characterized by a X-linked inheritance pattern.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
03/21/2017
MGI 6.08
The Jackson Laboratory