JSON

Charcot-Marie-Tooth disease type 4

^ http://purl.obolibrary.org/obo/MONDO_0018995

Charcot-Marie-Tooth disease type 4 (CMT4) belongs to the genetically heterogeneous group of CMT peripheral sensorimotor polyneuropathy diseases. [ Orphanet:64749 ]

Term info

database cross reference
  • Orphanet:64749 (MONDO:equivalentTo)
  • UMLS:CN043578 (MONDO:equivalentTo)
  • SCTID:715795005 (MONDO:equivalentTo)
  • GARD:0012440 (MONDO:equivalentTo)
  • DOID:0050541 (MONDO:equivalentTo)
Subsets

disease_grouping, ordo_group_of_disorders

abbreviation
CMT4 [ Orphanet:64749 ]

definition

Charcot-Marie-Tooth disease type 4 (CMT4) belongs to the genetically heterogeneous group of CMT peripheral sensorimotor polyneuropathy diseases.

exactMatch

http://linkedlifedata.com/resource/umls/id/CN043578, http://purl.obolibrary.org/obo/Orphanet_64749, http://purl.obolibrary.org/obo/DOID_0050541, http://identifiers.org/snomedct/715795005

has exact synonym

CMT4, autosomal recessive demyelinating Charcot-Marie-Tooth, AR-CMT1

id

MONDO:0018995