Human Disease and Mouse Model Detail
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Human Disease
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Pfeiffer Syndrome
OMIM ID: 101600
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Synonyms
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Acrocephalosyndactyly, Type V; ACS5;
Acs V
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View all models
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View ALL (2) 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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Fgfr1*
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FGFR1*
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View 1 model
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1:1 Homology
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Fgfr2*
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FGFR2*
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View 1 model
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1:1 Homology
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Mouse Models
Human Disease Modeled: Pfeiffer Syndrome
Associated Mouse Gene:
Fgfr1
Analysis Tools