Catalog
Charcot-Marie-Tooth disease 1 autosomal recessive
No MMS code
Link to WHO Definition
Charcot-Marie-Tooth disease 1 autosomal recessive – http://id.who.int/icd/entity/220263794
Charcot-Marie-Tooth disease type 4 (CMT4) belongs to the genetically heterogeneous group of Charcot-Marie-Tooth peripheral sensorimotor polyneuropathy diseases. It includes autosomal recessive, demyelinating forms of Charcot-Marie-Toothe disease.
Parents
Children
- Charcot-Marie-Tooth disease type 4A
- Charcot-Marie-Tooth disease type 4H
- Charcot-Marie-Tooth disease type 4E
- Charcot-Marie-Tooth disease type 4F
- Charcot-Marie-Tooth disease type 4C
- Charcot-Marie-Tooth disease type 4B2
- Charcot-Marie-Tooth disease type 4D
- Charcot-Marie-Tooth disease type 4B1
- Charcot-Marie-Tooth disease - deafness - intellectual deficit
- Charcot-Marie-Tooth disease type 4J
- Charcot-Marie-Tooth disease type 4G