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Human Disease and Mouse Model Detail
Human Disease Stuve-Wiedemann Syndrome
OMIM ID: 601559
Synonyms Schwartz-Jampel Syndrome, Neonatal; Schwartz-Jampel Syndrome, Type 2; SJS2; Stuve-Wiedemann/Schwartz-Jampel Type 2 Syndrome; STWS; SWS
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Lifr LIFR*   1:1 Homology

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
08/26/2014
MGI 5.19
The Jackson Laboratory