Hereditary motor and sensory neuropathy

Hereditary motor and sensory neuropathy (disorder)

active

Code	`398100001`
Semantic tag	disorder
Module	international
Definition	primitive
Effective time	20030731

Synonyms

CMT - Charcot-Marie-Tooth disease
HMSN - hereditary motor and sensory neuropathy
HSMN - hereditary sensory and motor neuropathy
Hereditary sensorimotor neuropathy
Hereditary sensory and motor neuropathy
Hereditary sensory-motor neuropathy

Parents (1)

65017003Hereditary peripheral neuropathy disorder

Children (38)

702439002Andermann syndrome disorder
765744006Autosomal dominant intermediate Charcot-Marie-Tooth disease type A disorder
765745007Autosomal dominant intermediate Charcot-Marie-Tooth disease type B disorder
765746008Autosomal dominant intermediate Charcot-Marie-Tooth disease type C disorder
765747004Autosomal dominant intermediate Charcot-Marie-Tooth disease type D disorder
722294004Autosomal dominant intermediate Charcot-Marie-Tooth disease type E disorder
770759001Autosomal dominant intermediate Charcot-Marie-Tooth disease type F disorder
778003000Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain disorder
764854006Autosomal dominant slowed nerve conduction velocity disorder
1187619001Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect disorder
773308001Autosomal recessive intermediate Charcot-Marie-Tooth disease type A disorder
773330000Autosomal recessive intermediate Charcot-Marie-Tooth disease type B disorder
773414009Autosomal recessive intermediate Charcot-Marie-Tooth disease type C disorder
1187567002Autosomal recessive intermediate Charcot-Marie-Tooth disease type D disorder
1222704008Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy disorder
715795005Charcot-Marie-Tooth disease type 4 disorder
763136000Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome disorder
398040009Charcot-Marie-Tooth disease, type I disorder
398187000Charcot-Marie-Tooth disease, type II disorder
1237626001Congenital axonal neuropathy with encephalopathy disorder
771261002Digital extensor muscle aplasia with polyneuropathy disorder
111499002Déjérine-Sottas disease disorder
715665006Hereditary motor and sensory neuropathy Okinawa type disorder
771143004Hereditary motor and sensory neuropathy type 5 disorder
771144005Hereditary motor and sensory neuropathy with acrodystrophy disorder
128203003Hereditary motor and sensory neuropathy with optic atrophy disorder
128204009Hereditary motor and sensory neuropathy with retinitis pigmentosa disorder
782881002Hereditary sensorimotor neuropathy with hyperelastic skin disorder
11442006Hereditary sensory neuropathy disorder
715645004Hereditary thermosensitive neuropathy disorder
1260129000Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome disorder
763798008Microcephalus, complex motor and sensory axonal neuropathy syndrome disorder
1172899000PMP22-RAI1 contiguous gene duplication syndrome disorder
1222646006Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome disorder
25362006Phytanic acid storage disease disorder
45853006Roussy-Lévy syndrome disorder
766977007Severe early-onset axonal neuropathy due to mitofusin 2 deficiency disorder
230552007X-linked hereditary motor and sensory neuropathy disorder