Autosomal dominant Charcot-Marie-Tooth disease type 2A1

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Name:
Autosomal dominant Charcot-Marie-Tooth disease type 2A1
Description:
A form of axonal Charcot-Marie-Tooth disease, a peripheral sensorimotor neuropathy, presenting with a more prominent muscle weakness in lower than upper limbs and frequent postural tremor.
ORPHAcode:
99946
Synonyms:
CMT2A1
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14