P699 | Disease Ontology ID | DOID:0050701 |
P2888 | exact match | http://identifiers.org/doid/DOID:0050701 |
http://purl.obolibrary.org/obo/DOID_0050701 | ||
P5270 | Mondo ID | MONDO_0000411 |
P5008 | on focus list of Wikimedia project | WikiProject Medicine | Q4099686 |
Q2346980 | absence seizure |
Q18553415 | adolescence-adult electroclinical syndrome |
Q18553414 | childhood electroclinical syndrome |
Q109835656 | developmental and epileptic encephalopathy |
Q18553413 | infancy electroclinical syndrome |
Q61913489 | infantile or early childhood epileptic encephalopathy 1 |
Q61913488 | infantile or early childhood epileptic encephalopathy 2 |
Q18553412 | neonatal period electroclinical syndrome |
Q18553416 | variable age at onset electroclinical syndrome |
Q87866917 | Absence status epilepsy: report of a rare electro-clinical syndrome |
Q67254922 | Ictal confusion — an electroclinical syndrome report of three adult cases with unusual features |
Q95491791 | Infantile spasms : electroclinical syndrome |
Q84287980 | Teaching Video NeuroImages: epilepsy with myoclonic absences: a distinct electroclinical syndrome |
Q51518288 | The evolving electroclinical syndrome of "epilepsy with ring chromosome 20". |
Q74022029 | [Pseudotumoral electroclinical syndrome of vascular origin; 9 observations] |
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