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ENParietal Foramina 1 (PFM1)
Alias:
Cranium Bifidum Occultum
Parietal Foramina, Symmetric
Foramina Parietalia Permagna
Cranium Bifidum, Hereditary
Catlin Marks
Pfm1
Pfm
Fpp
Enlarged Parietal Foramina
Foramina, Parietal
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Parietal Foramina 1, also known as cranium bifidum occultum, is related to frontonasal dysplasia 1 and frontofacionasal dysplasia, and has symptoms including headache and seizures. An important gene associated with Parietal Foramina 1 is MSX2 (Msh Homeobox 2). Affiliated tissues include bone and eye.
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Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
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Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
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Disease Model
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MGI
Related Gene
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References Literature
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IF
