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Human Disease and Mouse Model Detail
Human Disease Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1; MRXHF1
OMIM ID: 309580
Human Phenotype Ontology associations
Synonyms 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
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     ATRX* Atrx   HomoloGene and HGNC

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
MGI 6.07
The Jackson Laboratory