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hereditary motor and sensory neuropathy

Go to external page http://purl.obolibrary.org/obo/MONDO_0015358

A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-Tooth DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343) [ MESH:D015417 ]

Synonyms: HMSN

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:140450 (MONDO:equivalentObsolete)
  • SCTID:398100001 (MONDO:equivalentTo)
  • MESH:D015417 (Orphanet:140450/e)
Subsets

disease_grouping, rare, orphanet_rare, ordo_group_of_disorders

exactMatch

http://identifiers.org/snomedct/398100001

http://identifiers.org/mesh/D015417

id

MONDO:0015358

Term relations