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Human Disease and Mouse Model Detail
Human Disease Weill-Marchesani Syndrome 2; WMS2
OMIM ID: 608328
Synonyms Glaucoma-Lens Ectopia-Microspherophakia-Stiffness-Shortness Syndrome; GEMSS; Mesodermal Dysmorphodystrophy, Congenital; Spherophakia-Brachymorphia Syndrome; Weill-Marchesani Syndrome; Weill-Marchesani Syndrome, Autosomal Dominant
View all models View ALL (2) mouse models for this human disease.
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
     Fbn1* FBN1* View 2 models 1:1 Homology
References Disease References using Mouse Models (1)

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
07/15/2014
MGI 5.18
The Jackson Laboratory