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Human Disease and Mouse Model Detail
Human Disease Ulna and Fibula, Absence of, with Severe Limb Deficiency
OMIM ID: 276820
Human Phenotype Ontology associations
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...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     WNT7A* Wnt7a   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