Human Disease and Mouse Model Detail
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Human Disease
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Feingold Syndrome 2; FGLDS2
OMIM ID: 614326
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Synonyms
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Brachydactyly with Short Stature and Microcephaly
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View all models
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View ALL (1) mouse models for this human disease.
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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MIR17HG*
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Transgenes and
other genome features
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Transgenes and other genome features developed in mice to model this disease.
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Mouse Models
Human Disease Modeled: Feingold Syndrome 2; FGLDS2
Associated Mouse Complex/Cluster/Region:
Mirc1
Analysis Tools