loading...| Preferred Name |
hereditary motor and sensory neuropathy |
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| Synonyms |
HMSN |
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| Definitions |
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) |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0015358 |
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| database_cross_reference |
COHD:4134552 SCTID:398100001 MESH:D015417 ICD10:G60.0 GARD:0012685 Orphanet:140450 |
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| exactMatch |
http://identifiers.org/mesh/D015417 http://www.orpha.net/ORDO/Orphanet_140450 |
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| has exact synonym |
HMSN |
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| id |
MONDO:0015358 |
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| imported from | ||
| in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders |
|
| label |
hereditary motor and sensory neuropathy |
|
| notation |
MONDO:0015358 |
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| prefLabel |
hereditary motor and sensory neuropathy |
|
| textual definition |
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) |
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| subClassOf |