encephalopathy due to GLUT1 deficiency
disease
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encephalopathy due to GLUT1 deficiency
Summary
encephalopathy due to GLUT1 deficiency is a designated intractable/rare disease[1]. It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- encephalopathy due to GLUT1 deficiency's instance of is recorded as designated intractable/rare disease[3].
- encephalopathy due to GLUT1 deficiency's instance of is recorded as rare disease[4].
- encephalopathy due to GLUT1 deficiency's instance of is recorded as class of disease[5].
- encephalopathy due to GLUT1 deficiency is a type of encephalopathy[6].
- encephalopathy due to GLUT1 deficiency is a type of genetic disease[7].
- encephalopathy due to GLUT1 deficiency is a type of neurometabolic disease[8].
- encephalopathy due to GLUT1 deficiency is a type of glucose transport disorder[9].
- encephalopathy due to GLUT1 deficiency is a type of other metabolic disease with epilepsy[10].
- encephalopathy due to GLUT1 deficiency's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4453[11].
- encephalopathy due to GLUT1 deficiency's NCI Thesaurus ID is recorded as C168599[12].
- encephalopathy due to GLUT1 deficiency's health specialty is recorded as medical genetics[13].
- encephalopathy due to GLUT1 deficiency's genetic association is recorded as GLUT1[14].
- encephalopathy due to GLUT1 deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_71277[15].
Why It Matters
encephalopathy due to GLUT1 deficiency has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[2] It is known by 25 alternative names across languages and contexts.[16]