| Human Disease |
Mental Retardation, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity; MEHMO OMIM ID: 300148 |
| Synonyms | Mental Retardation, X-Linked, Syndromic 20; MRXS20; Mental Retardation, X-Linked, Syndromic 25; MRXS25 |
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Genes and mouse models |
There are currently no human or mouse genes associated with this disease in the MGI database. |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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