childhood onset GLUT1 deficiency syndrome 2
0 sources
childhood onset GLUT1 deficiency syndrome 2
Summary
childhood onset GLUT1 deficiency syndrome 2 is a rare disease[1]. It draws 49 Wikipedia views per month (rare_disease category, ranking #236 of 627).[2]
Key Facts
- childhood onset GLUT1 deficiency syndrome 2's instance of is recorded as rare disease[3].
- childhood onset GLUT1 deficiency syndrome 2's instance of is recorded as class of disease[4].
- childhood onset GLUT1 deficiency syndrome 2 is a type of Paroxysmal dyskinesia[5].
- childhood onset GLUT1 deficiency syndrome 2 is a type of dystonia[6].
- childhood onset GLUT1 deficiency syndrome 2 is a type of genetic disease[7].
- childhood onset GLUT1 deficiency syndrome 2 is a type of autosomal dominant disease[8].
- childhood onset GLUT1 deficiency syndrome 2's health specialty is recorded as neurology[9].
- childhood onset GLUT1 deficiency syndrome 2's genetic association is recorded as GLUT1[10].
- childhood onset GLUT1 deficiency syndrome 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0090045[11].
- childhood onset GLUT1 deficiency syndrome 2's exact match is recorded as http://identifiers.org/doid/DOID:0090045[12].
- childhood onset GLUT1 deficiency syndrome 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_98811[13].
- childhood onset GLUT1 deficiency syndrome 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
childhood onset GLUT1 deficiency syndrome 2 draws 49 Wikipedia views per month (rare_disease category, ranking #236 of 627).[2]