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isolated hereditary congenital facial paralysis

Disease Summary
Associated Targets ()

Mondo Description Isolated hereditary congenital facial paralysis (IHCFP) is an extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve and has been reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or asymmetrical facial palsy. Involvement of the branches of the facial nerve can be unequal.
Mondo Term and Equivalent IDs
MONDO:0011090:  isolated hereditary congenital facial paralysis
GARD:0008583: 
MESH:C563309: 
OMIMPS:601471: 
Orphanet:306527: 
SCTID:733091002: 
UMLS:C4518577: