| Human Disease |
Chondrodysplasia, Grebe Type OMIM ID: 200700 |
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| Synonyms | Achondrogenesis, Brazilian; Achondrogenesis, Type II, Formerly; Acromesomelic Dysplasia, Grebe Type; AMDG; Grebe Chondrodysplasia; Grebe Dysplasia | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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