pyridoxine-dependent epilepsy
extremely rare disorder
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pyridoxine-dependent epilepsy
Summary
pyridoxine-dependent epilepsy is a rare disease[1].
Key Facts
- pyridoxine-dependent epilepsy's instance of is recorded as rare disease[2].
- pyridoxine-dependent epilepsy's instance of is recorded as class of disease[3].
- pyridoxine-dependent epilepsy is a type of epilepsy[4].
- pyridoxine-dependent epilepsy is a type of neurometabolic disease[5].
- pyridoxine-dependent epilepsy is a type of disorder of pyridoxine metabolism[6].
- pyridoxine-dependent epilepsy is a type of rare genetic epilepsy[7].
- pyridoxine-dependent epilepsy is a type of metabolic neurotransmission anomaly with epilepsy[8].
- pyridoxine-dependent epilepsy is a type of autosomal recessive disease[9].
- pyridoxine-dependent epilepsy's health specialty is recorded as neurology[10].
- pyridoxine-dependent epilepsy's genetic association is recorded as ALDH7A1[11].
- pyridoxine-dependent epilepsy's genetic association is recorded as PLPBP[12].
- pyridoxine-dependent epilepsy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3006[13].
- pyridoxine-dependent epilepsy's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080768[14].
- pyridoxine-dependent epilepsy's exact match is recorded as http://identifiers.org/doid/DOID:0080768[15].