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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.
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Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
GARD:0008583
MESH:C563309
OMIMPS:601471
Orphanet:306527
SCTID:733091002
UMLS:C4518577
MONDO:0011090
High level summary of knowledge for a disease, including descriptions and datasource references.