Human Disease and Mouse Model Detail
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Human Disease
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Hypochondroplasia; HCH
OMIM ID: 146000
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View all models
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View ALL (1) "NOT" mouse models for this human disease.
No mouse models with similarity to the expected human disease phenotype are reported in MGI.
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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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Fgfr3
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FGFR3*
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View 1 "NOT" model
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1:1 Homology
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Mouse Models
Human Disease Modeled: Hypochondroplasia; HCH
NOT Models
No similarity to the expected human disease phenotype was found.
Analysis Tools