ERMN
Description
The ERMN (ermin) is a protein-coding gene located on chromosome 2.
ERMN is also known as JN, KIAA1189.
Associated Diseases
- Charcot-Marie-Tooth disease type 1A
- Charcot-Marie-Tooth disease type 1C
- autosomal dominant slowed nerve conduction velocity
- Charcot-Marie-Tooth disease type 4J
- hereditary neuropathy with liability to pressure palsies
- Charcot-Marie-Tooth disease type 1F
- hypertriglyceridemia 2
- Charcot-Marie-Tooth disease type 4A
- cholesterol-ester transfer protein deficiency
- Charcot-Marie-Tooth disease type 1B
- null syndrome
- Charcot-Marie-Tooth disease axonal type 2L
- Charcot-Marie-Tooth disease type 4G
- Charcot-Marie-Tooth disease type 2A1
