facial neuralgia
Also known as: facial nerve neuralgia, neuralgia of facial nerve
Additional Disease Briefs
facial onset sensory and motor neuronopathy
Also known as: FOSMN syndrome, facial onset sensorimotor neuronopathy syndrome, facial onset sensory and motor neuronopathy syndrome
facial paresis, hereditary congenital, 1
Also known as: HCFP1, Mobius syndrome 2, Mobius syndrome 2, formerly, Moebius syndrome 2, Moebius syndrome 2, formerly, facial palsy, congenital, unilateral or bilateral, facial paresis, hereditary congenital, 1
facial paresis, hereditary congenital, 2
Also known as: HCFP2, Mobius syndrome 3, Mobius syndrome 3, formerly, Moebius syndrome 3, Moebius syndrome 3, formerly, facial paresis, hereditary congenital, 2
facial paresis, hereditary congenital, 3
Also known as: HCFP3, HOXB1 congenital hereditary facial paralysis-variable hearing loss syndrome, congenital hereditary facial paralysis-variable hearing loss syndrome caused by mutation in HOXB1, facial paresis, hereditary congenital, 3, facial paresis, hereditary congenital, type 3
faciocardiorenal syndrome
Also known as: Eastman Bixler syndrome, Eastman-Bixler syndrome, faciocardiorenal syndrome
facioscapulohumeral muscular dystrophy 1
Also known as: FMD, FRG1 facioscapulohumeral muscular dystrophy, FSHD, FSHD1, FSHD1A, FSHMD1A, Landouzy-Dejerine muscular dystrophy, Landouzy-Dejerine muscular dystrophy facioscapulohumeral muscular dystrophy, infantile, included, facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles, facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles, included, facioscapulohumeral muscular dystrophy, facioscapulohumeral muscular dystrophy 1, facioscapulohumeral muscular dystrophy 1A, facioscapulohumeral muscular dystrophy caused by mutation in FRG1, facioscapulohumeral muscular dystrophy type 1, facioscapulohumeral muscular dystrophy, infantile, muscular dystrophy, facioscapulohumeral, muscular dystrophy, facioscapulohumeral, type 1, muscular dystrophy, facioscapulohumeral, type 1A
facioscapulohumeral muscular dystrophy 2
Also known as: FSHD2, Fshd2, digenic, SMCHD1 facioscapulohumeral muscular dystrophy, facioscapulohumeral muscular dystrophy 2, facioscapulohumeral muscular dystrophy 2, digenic, facioscapulohumeral muscular dystrophy caused by mutation in SMCHD1, facioscapulohumeral muscular dystrophy type 2, fascioscapulohumeral muscular dystrophy 2, digenic, digenic dominant, muscular dystrophy, facioscapulohumeral, type 1B, muscular dystrophy, facioscapulohumeral, type 2
facioscapulohumeral muscular dystrophy 3, digenic
Also known as: FSHD3, facioscapulohumeral muscular dystrophy 3, digenic