About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Ulna and Fibula, Absence of, with Severe Limb Deficiency
OMIM ID: 276820
Synonyms Al-Awadi/Raas-Rothschild Syndrome; AARRS; Limb/Pelvis-Hypoplasia/Aplasia Syndrome; LPHAS; Schinzel Phocomelia 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...
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Wnt7a WNT7A*   1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 5.21
The Jackson Laboratory