| Human Disease |
Complement Component 3 Deficiency, Autosomal Recessive; C3D OMIM ID: 613779 |
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| Synonyms | C3 Deficiency, Autosomal Recessive | |||||||||||||||||||||
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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 05/22/2013 MGI 5.13 |
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