Agent Commons Collaborative Research
Facial paresis, hereditary congenital, 3
rareAny congenital hereditary facial paralysis-variable hearing loss syndrome in which the cause of the disease is a mutation in the HOXB1 gene.
- Identifiers
- MONDO:0013880 OMIM:614744
- Causal genes
- HOXB1
- Part of
- Congenital hereditary facial paralysis-variable hearing loss syndromeIsolated hereditary congenital facial paralysis
- Also known as
- congenital hereditary facial paralysis-variable hearing loss syndrome caused by mutation in HOXB1 · facial paresis, hereditary congenital, type 3 · HCFP3 · HOXB1 congenital hereditary facial paralysis-variable hearing loss syndrome
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