Human Disease and Mouse Model Detail
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Human Disease
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Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1; MRXHF1
OMIM ID: 309580
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Synonyms
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Carpenter-Waziri Syndrome;
Chudley-Lowry Syndrome;
Holmes-Gang Syndrome;
Juberg-Marsidi Syndrome; JMS;
Mental Retardation, X-Linked, with Growth Retardation, Deafness, and Microgenitalism;
Sfms;
Smith-Fineman-Myers Syndrome 1; SFM1;
Xlmr-Hypotonic Facies Syndrome
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Atrx
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ATRX*
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1:1 Homology
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Analysis Tools