pyridoxine-dependent epilepsy

Summary

pyridoxine-dependent epilepsy is a rare disease^[1]. It draws 5 Wikipedia views per month (rare_disease category, ranking #233 of 627).^[2]

Key Facts

• pyridoxine-dependent epilepsy's instance of is recorded as rare disease^[3].
• pyridoxine-dependent epilepsy's instance of is recorded as class of disease^[4].
• pyridoxine-dependent epilepsy's subclass of is recorded as epilepsy^[5].
• pyridoxine-dependent epilepsy's subclass of is recorded as neurometabolic disease^[6].
• pyridoxine-dependent epilepsy's subclass of is recorded as disorder of pyridoxine metabolism^[7].
• pyridoxine-dependent epilepsy's subclass of is recorded as rare genetic epilepsy^[8].
• pyridoxine-dependent epilepsy's subclass of is recorded as metabolic neurotransmission anomaly with epilepsy^[9].
• pyridoxine-dependent epilepsy's subclass of is recorded as autosomal recessive disease^[10].
• pyridoxine-dependent epilepsy's MeSH descriptor ID is recorded as C536254^[11].
• pyridoxine-dependent epilepsy's OMIM ID is recorded as 266100^[12].
• pyridoxine-dependent epilepsy's KEGG ID is recorded as H01247^[13].
• pyridoxine-dependent epilepsy's eMedicine ID is recorded as 985667^[14].
• pyridoxine-dependent epilepsy's Disease Ontology ID is recorded as DOID:0080768^[15].
• pyridoxine-dependent epilepsy's Orphanet ID is recorded as 3006^[16].
• pyridoxine-dependent epilepsy's health specialty is recorded as neurology^[17].
• pyridoxine-dependent epilepsy's genetic association is recorded as ALDH7A1^[18].
• pyridoxine-dependent epilepsy's genetic association is recorded as PLPBP^[19].
• pyridoxine-dependent epilepsy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3006^[20].
• pyridoxine-dependent epilepsy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080768^[21].
• pyridoxine-dependent epilepsy's exact match is recorded as http://identifiers.org/doid/DOID:0080768^[22].
• pyridoxine-dependent epilepsy's UMLS CUI is recorded as C1849508^[23].
• pyridoxine-dependent epilepsy's UMLS CUI is recorded as C1291560^[24].
• pyridoxine-dependent epilepsy's ICD-10-CM is recorded as G40.8^[25].
• pyridoxine-dependent epilepsy's GARD rare disease ID is recorded as 9298^[26].
• pyridoxine-dependent epilepsy's Mondo ID is recorded as MONDO_0009945^[27].

Why It Matters

pyridoxine-dependent epilepsy draws 5 Wikipedia views per month (rare_disease category, ranking #233 of 627).^[2]