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Term:
Hereditary Sensorimotor Neuropathy with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance
(DOID:9003541)
Annotations:
Rat: (0)
Mouse: (0)
Human: (0)
Chinchilla: (0)
Bonobo: (0)
Dog: (0)
Squirrel: (0)
Pig: (0)
Parent Terms
Term With Siblings
Child Terms
eye disease
+
motor neuron disease
+
motor peripheral neuropathy
+
Riley-Day syndrome
+
AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME
Aland Island eye disease
Alstrom syndrome
amblyopia
+
ancylostomiasis
+
Asthenopia
baylisascariasis
blindness
+
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods
Cerebellar, Ocular, Craniofacial, and Genital Syndrome
Charcot-Marie-Tooth disease
+
Cogan syndrome
+
Congenital Anterior Cervical Hypertrichosis with Peripheral Sensory and Motor Neuropathy
conjunctival disease
+
corneal disease
+
cysticercosis
+
dipetalonemiasis
distal hereditary motor neuronopathy type 7
+
Encephalocraniocutaneous Lipomatosis
essential tremor 2
Eye Abnormalities
+
eye accommodation disease
+
eye degenerative disease
+
Eye Hemorrhage
+
Eye Infections
+
Eye Injuries
+
Eye Manifestations
+
Eye Neoplasms
+
eyelid disease
+
fundus dystrophy
+
Giant Axonal Neuropathy
+
glaucoma
+
globe disease
+
gonorrhea
+
Hagemoser Weinstein Bresnick Syndrome
Hereditary Eye Diseases
+
Hereditary Motor and Sensory Neuropathy with Excessive Myelin Folding Complex, Autosomal Recessive
hereditary neuropathy with liability to pressure palsies
Hereditary Sensorimotor Neuropathy with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance
Hereditary Sensory Neuropathy with Spastic Paraplegia, Autosomal Recessive
hereditary spastic paraplegia
+
Hereditary Thermosensitive Neuropathy
Hernandez Fragoso Syndrome
lacrimal apparatus disease
+
lateral sclerosis
lens disease
+
leprosy
+
loiasis
Marfan syndrome
+
microphthalmia
+
Mollica Pavone Antener Syndrome
MORM Syndrome
motor neuritis
+
MOTOR NEURON ATROPHY
+
Motor Neuron Disease with Dementia and Ophthalmoplegia
multisystem proteinopathy
NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES
NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME
Neuromuscular Oculoauditory Syndrome
nonparalytic poliomyelitis
ocular albinism
+
ocular hypertension
+
ocular hypotension
+
ocular motility disease
+
Ocular Neovascularization
+
ophthalmia nodosa
ophthalmomyiasis
optic nerve disease
+
orbital disease
+
philophthalmiasis
poliomyelitis
+
Polyneuropathy, Lethal Neonatal, Axonal Sensorimotor, Autosomal Recessive
Primary Lateral Sclerosis Juvenile
progressive bulbar palsy
+
progressive muscular atrophy
pseudobulbar palsy
+
pupil disease
+
refractive error
+
Refsum disease
+
retinal disease
+
scleral disease
+
scotoma
+
sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
Slowed Nerve Conduction Velocity, Autosomal Dominant
spinal muscular atrophy
+
SPOAN syndrome
Tamari Goodman Syndrome
toxocariasis
+
uveal disease
+
Vision Disorders
+
visual pathway disease
+
vitreous detachment
+
vitreous disease
+
Synonyms
Primary IDs:
MESH:C563517
Alternate IDs:
OMIM:162380