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facial paresis, hereditary congenital, 3 | RareConnect | RareConnect.io

/hereditary disease

/congenital hereditary facial paralysis-variable hearing loss syndrome

/facial paresis, hereditary congenital, 3

facial paresis, hereditary congenital, 3

Rare Disease

MONDO:0013880

Also Known As

HOXB1 congenital hereditary facial paralysis-variable hearing loss syndromecongenital hereditary facial paralysis-variable hearing loss syndrome caused by mutation in HOXB1facial paresis, hereditary congenital, 3facial paresis, hereditary congenital, type 3HCFP3

Definition

Any congenital hereditary facial paralysis-variable hearing loss syndrome in which the cause of the disease is a mutation in the HOXB1 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:614744 ↗

GARD

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