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loading...| Preferred Name | monogenic epilepsy | |
| Synonyms |
monogenic disease with epilepsy |
|
| ID |
http://purl.obolibrary.org/obo/MONDO_0015653 |
|
| database_cross_reference |
GARD:20086 Orphanet:166472 |
|
| exactMatch | ||
| has characteristic | ||
| has_exact_synonym |
monogenic disease with epilepsy |
|
| id |
MONDO:0015653 |
|
| in_subset |
http://purl.obolibrary.org/obo/mondo#rare http://purl.obolibrary.org/obo/mondo#gard_rare http://purl.obolibrary.org/obo/mondo#disease_grouping http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders |
|
| label |
monogenic epilepsy |
|
| notation |
MONDO:0015653 |
|
| prefLabel |
monogenic epilepsy |
|
| treeView | ||
| subClassOf |
Create mapping
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.obolibrary.org/obo/MONDO_0015653 | CCONT | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0015653 | EFO | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0015653 | EFO | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0015653 | DOVES | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0015653 | KTAO | SAME_URI | |
| http://purl.obolibrary.org/obo/MONDO_0015653 | CCONT | LOOM | |
| http://purl.obolibrary.org/obo/MONDO_0015653 | EFO | LOOM | |
| http://purl.obolibrary.org/obo/MONDO_0015653 | EFO | LOOM | |
| http://purl.obolibrary.org/obo/MONDO_0015653 | DOVES | LOOM | |
| http://purl.obolibrary.org/obo/MONDO_0015653 | KTAO | LOOM |