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Ontology Browser
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) Naked Mole-rat: (0) Green Monkey: (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  
Alstrom syndrome  
amblyopia +   
ancylostomiasis +  
anterior horn cell disease 
Asthenopia  
autosomal dominant distal hereditary motor neuronopathy 7  
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 
Encephalocraniocutaneous Lipomatosis  
essential tremor 2 
Eye Abnormalities +   
eye accommodation disease +  
eye adnexa 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 hypertension +   
ocular hypotension +   
ocular motility disease +   
Ocular Neovascularization +   
ocular sarcoidosis  
ophthalmia nodosa 
ophthalmomyiasis 
optic nerve disease +   
orbital disease +   
PERIPHERAL MOTOR NEUROPATHY, CHILDHOOD-ONSET, BIOTIN-RESPONSIVE  
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: MIM:162380

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