MeSH Treeview
Query OMIM entry list
148360
-
KERATODERMA, PALMOPLANTAR, WITH NAIL DYSTROPHY AND HEREDITARY MOTOR-SENSORY NEUROPATHY
→
High-scoring List
Musculoskeletal Diseases
Muscular Diseases
Muscle Spasticity
Nervous System Diseases
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Spasticity
Muscular Atrophy
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Skin Diseases, Genetic
Keratoderma, Palmoplantar
Skin and Connective Tissue Diseases
Skin Diseases
Keratosis
Keratoderma, Palmoplantar
Skin Diseases, Genetic
Keratoderma, Palmoplantar
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Muscular Atrophy
Nails, Malformed
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Spasticity
Muscular Atrophy
Database Center for Life Science
