Human Disease and Mouse Model Detail
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Human Disease
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Parietal Foramina; PFM
OMIM ID: 168500
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Synonyms
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Catlin Marks;
Cranium Bifidum Occultum;
Foramina Parietalia Permagna; FPP;
Parietal Foramina, Symmetric
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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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Msx2*
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MSX2*
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View 1 model
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1:1 Homology
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Mouse Models
Human Disease Modeled: Parietal Foramina; PFM
Associated Mouse Gene:
Msx2
Analysis Tools