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Human Disease and Mouse Model Detail
Human Disease Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type
OMIM ID: 271665
Human Phenotype Ontology associations
Synonyms Smed, Short Limb-Abnormal Calcification Type; SMED, Short Limb-Hand Type; SMED, Type II; Smed-Sl; Smed-Sl/Ac; Spondylometaepiphyseal Dysplasia, Short Limb-Abnormal Calcification Type
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
     DDR2* Ddr2   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