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ENFacial Paresis, Hereditary Congenital, 3 (HCFP3)
Alias:
Hcfp3
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Facial Paresis, Hereditary Congenital, 3, is also known as hcfp3. An important gene associated with Facial Paresis, Hereditary Congenital, 3 is HOXB1 (Homeobox B1). Affiliated tissues include eye, and related phenotypes are esophoria and facial palsy
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Basic Information
Inheritance
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MALACARDS
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HPO Frequency
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MGI
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IF
