MeSH Treeview
Query OMIM entry list
162380
-
NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUAL PATHWAY AND AUTONOMIC DISTURBANCE
→
High-scoring List
Nervous System Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Autonomic Nervous System Diseases
Primary Dysautonomias
Dysautonomia, Familial
Demyelinating Diseases
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Nervous System Malformations
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Immune System Diseases
Autoimmune Diseases
Autoimmune Diseases of the Nervous System
Polyradiculoneuropathy
Hereditary Sensory and Autonomic Neuropathies
Dysautonomia, Familial
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Pathologic Processes
Disease
Syndrome
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscular Atrophy
Database Center for Life Science