Charcot–Marie–Tooth disease

neuromuscular disease that is characterized by a slowly progressive degeneration of the muscles of the foot, lower leg, hand and forearm

Wikidata entity: Q1052687

Wikimedia Commons category is Charcot-Marie-Tooth disease

Quantities

P1193prevalence0.0003

P373 Commons category String Charcot-Marie-Tooth disease ???
P2888 exact match Url Ontology Lookup Service (OLS) ???
P2888 exact match Url Disease Ontology - Institute for Genome Sciences @ University of Maryland ???
P1325 external data available at URL Url None ???
P2293 genetic association ... Q14912888 (MPZ) MPZ
P2293 genetic association ... Q18025986 (GJB1) GJB1
P2293 genetic association ... Q18030619 (PMP22) PMP22
P828 has cause ... Q42918 (mutation) mutation
P1995 health specialty ... Q83042 (neurology) neurology
P1692 ICD-9-CM String 356.1 ???
P31 instance of ... Q42303753 (designated intractable/rare disease) designated intractable/rare disease
P31 instance of ... Q112193867 (class of disease) class of disease
P31 instance of ... Q929833 (rare disease) rare disease
P923 medical examination ... Q64830627 (neurological diagnostic techniques) neurological diagnostic techniques
P923 medical examination ... Q285223 (genetic testing) genetic testing
P923 medical examination ... Q507369 (electromyography) electromyography
P138 named after ... Q20710 (Jean-Martin Charcot) Jean-Martin Charcot
P138 named after ... Q11710166 (Howard Henry Tooth) Howard Henry Tooth
P138 named after ... Q609441 (Pierre Marie) Pierre Marie
P1748 NCI Thesaurus ID String C75467 ???
P5008 on focus list of Wikimedia project ... Q4099686 (WikiProject Medicine) WikiProject Medicine
P924 possible treatment ... Q186005 (physiotherapy) physiotherapy
P924 possible treatment ... Q24238356 (unknown) unknown
P279 subclass of ... Q12136 (disease) disease
P279 subclass of ... Q15270307 (hereditary motor and sensory neuropathy) hereditary motor and sensory neuropathy
P279 subclass of ... Q1225194 (monogenic disease) monogenic disease
P279 subclass of ... Q2246789 (neuromuscular disease) neuromuscular disease
P780 symptoms and signs ... Q270421 (muscle weakness) muscle weakness
P780 symptoms and signs ... Q174857 (scoliosis) scoliosis
P780 symptoms and signs ... Q2289481 (sensory loss) sensory loss
P780 symptoms and signs ... Q1419356 (hyporeflexia) hyporeflexia
P780 symptoms and signs ... Q1557686 (muscle atrophy) muscle atrophy
P780 symptoms and signs ... Q1624054 (pes cavus) pes cavus
External Ids
P2581BabelNet ID00017784n
P2581BabelNet ID00017784n
P268Bibliothèque nationale de France ID122665167
P508BNCF Thesaurus ID52644
P699Disease Ontology IDDOID:10595
P557DiseasesDB2343
P557DiseasesDB5815
P673eMedicine ID1232386
P673eMedicine ID315260
P1417Encyclopædia Britannica Online IDscience/Charcot-Marie-Tooth-disease
P646Freebase ID/m/0268d
P4317GARD rare disease ID6034
P7464Genetics Home Reference Conditions IDcharcot-marie-tooth-disease
P4229ICD-10-CMG60.0
P665KEGG IDH00264
P244Library of Congress authority IDsh85022641
P604MedlinePlus ID000727
P604MedlinePlus ID000727
P486MeSH descriptor IDD002607
P672MeSH tree codeC10.500.300.200
P672MeSH tree codeC10.574.500.495.200
P672MeSH tree codeC10.668.829.800.300.200
P672MeSH tree codeC16.131.666.300.200
P672MeSH tree codeC16.320.400.375.200
P6366Microsoft Academic ID (discontinued)2910997174
P8189National Library of Israel J9U ID987007284792605171
P7995NHS Health A to Z IDcharcot-marie-tooth-disease
P492OMIM ID311860
P492OMIM ID311860
P1550Orphanet ID166
P4233PatientsLikeMe condition IDcharcot-marie-tooth
P5082Store medisinske leksikon IDCharcot-Marie-Tooths_sykdom
P4527UK Parliament thesaurus ID9073
P2892UMLS CUIC0007959
P11143WikiProjectMed IDCharcot–Marie–Tooth disease
P3471WikiSkripta article ID22034
P13591Yale LUX IDconcept/8d5fa112-06d2-4072-9dc2-38f75ed72fa8
P2347YSO ID12273

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