CUI ⟾ or DBPEDIA ⟾
Ex: C0006933 C0007102 C0007203 C3175196    or    http://dbpedia.org/resource/Nosebleed    http://dbpedia.org/resource/Leg

CUI: C0007959   Charcot-Marie-Tooth Disease 
A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343)

rdfs:seeAlso —
http://dbpedia.org/resource/Vector_(epidemiology) C0012656 C0021573 C1690019
http://dbpedia.org/resource/Disease C0000768 C0006111 C0015127 C0205269 C0231218 C1314792 C1331418 C1457887 C0012634 C0026538 C0178685 C0221423 C0231172 C0679215 C0683323 C0683324 C0683337 C0699749 C1514815 C2359469 C3540542
http://dbpedia.org/resource/Atrophy C0151514 C0333641
http://dbpedia.org/resource/Heredity C0019266 C0265388 C0439660 C0678919 C0728826
http://dbpedia.org/resource/Muscle_atrophy C0026848 C0026846 C0752352
http://dbpedia.org/resource/Tooth C0040426 C0040452 C0227028 C2004463
http://dbpedia.org/resource/Dominance_(genetics) C0017342 C0017361 C0178491 C0178492 C0441748 C0443147 C0678942 C0683222 C0683223 C1527180 C3899988 C3899989
http://dbpedia.org/resource/Hereditary_motor_and_sensory_neuropathy C0027888
http://dbpedia.org/resource/Genetic_disorder C1704258 C0019247 C0206530 C0262496 C0277558 C0683231 C0950123 C1704257 C2924406
http://dbpedia.org/resource/Muscle C0026832 C0026845 C0026848 C0027664 C0240417 C0442025 C0517349 C1704336 C1995013
http://dbpedia.org/resource/Syndrome C1332133 C0039082 C0567439
http://dbpedia.org/resource/Peripheral_neuropathy C0259749 C0027813 C0031117 C0032541 C0151295 C0151313 C0235025 C0235026 C0235880 C0392553 C0442874 C0494491 C0740343 C1522415

skos:closeMatch —

skos:exactMatch —
http://dbpedia.org/resource/Charcot–Marie–Tooth_disease C0007959 C0011195 C0044232 C0270911 C0270912 C0270913 C0393807 C0393808 C0795910 C1423872 C1427281 C1832274 C1832334 C1832399 C1833219 C1836336 C1837552 C1839566 C1843153 C1843164 C1843225 C1843247 C1844864 C1854150 C1854154 C1859198 C1861668 C1866636 C1970011 C2079538 C2079540 C2931686 C3811170


UMLS Concepts to DBPedia Link Discovery Browser


Enter an UMLS concept-unique-identifier (CUI) or DBPEDIA resource uri to show its rdfs:seeAlso, skos:closeMatch, and skos:exactMatch mapped relations to DBpedia. Alternatively, you can click on a CUI from the sample list to the right to compare our mapping to Wikidata.