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bn:00017784n
Noun Concept
SYL
No term available
EN
A form of neuropathy that can begin between childhood and young adulthood; characterized by weakness and atrophy of the muscles of the hands and lower legs; progression is slow and individuals affected can have a normal life span; inheritance is X-linked recessive or X-linked dominant WordNet 3.0
Relations
Sources
IS A
EN
neuropathy
EN
disease
EN
rare disease
EN
birth defect
EN
Charcot-Marie-Tooth disease
+2 relations
HAS KIND
EN
Charcot-Marie-Tooth disease
EN
Alström syndrome
EN
Dejerine–Sottas disease
EN
Charcot-Marie-Tooth disease type 1
EN
Charcot-Marie-Tooth disease type 2
+6 relations
GENETIC ASSOCIATION
EN
myelin protein zero
EN
GJB1
EN
peripheral myelin protein 22
HAS CAUSE
EN
mutation
HEALTH SPECIALTY
EN
neurology
MEDICAL EXAMINATIONS
EN
electromyography
EN
genetic screening
NAMED AFTER
EN
Charcot
Pierre marie
EN
Howard Henry Tooth
POSSIBLE TREATMENT
EN
physical therapy
SYMPTOMS
EN
clawfoot
EN
myasthenia
EN
scoliosis
EN
muscle atrophy
EN
sensory loss
+1 relations

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