Preferred Name

Hereditary motor and sensory neuropathy

Synonyms

Peroneal muscular atrophy (axonal type) (hypertrophic type)

ID

http://purl.bioontology.org/ontology/ICD10CM/G60.0

altLabel

Peroneal muscular atrophy (axonal type) (hypertrophic type)

Hereditary motor and sensory neuropathy, types I-IV

Hypertrophic neuropathy of infancy

Charcot-Marie-Tooth disease

Roussy-Levy syndrome

Déjérine-Sottas disease

cui

C0027888

C1408174

C0011195

C0205713

C0007959

C2875300

C1408182

notation

G60.0

Order number

06665

prefLabel

Hereditary motor and sensory neuropathy

tui

T047

subClassOf

http://purl.bioontology.org/ontology/ICD10CM/G60

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http://purl.bioontology.org/ontology/MEDLINEPLUS/C0027888 MedlinePlus Health Topics / MedlinePlus网站健康主题 CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0027888 MedlinePlus Health Topics / MedlinePlus网站健康主题 LOOM
http://purl.bioontology.org/ontology/OMIM/601097 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/145900 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0007959 MedlinePlus Health Topics / MedlinePlus网站健康主题 CUI
http://purl.bioontology.org/ontology/MESH/D002607 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/D002607 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/ICD10/G60.0 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bioontology.org/ontology/ICD10/G60.0 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.bioontology.org/ontology/MESH/D015417 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/D015417 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/OMIM/118200 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bmicc.cn/ontology/ICD10CN/G60.0 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/OMIM/180800 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/304040 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.bioontology.org/ontology/OMIM/159440 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 CUI
http://purl.obolibrary.org/obo/MONDO_0015358 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0015358 Experimental Factor Ontology / 实验性因素本体 LOOM