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isolated hereditary congenital facial paralysis

Disease Summary
Associated Targets (0)

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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: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found