Infantile convulsions and choreoathetosis

medical condition
MedicalCondition rare_disease Q6029036
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Summary

Infantile convulsions and choreoathetosis is a rare disease[1].

Key Facts

  • Infantile convulsions and choreoathetosis's instance of is recorded as rare disease[2].
  • Infantile convulsions and choreoathetosis's instance of is recorded as class of disease[3].
  • Infantile convulsions and choreoathetosis's subclass of is recorded as Paroxysmal dyskinesia[4].
  • Infantile convulsions and choreoathetosis's subclass of is recorded as Benign infantile epilepsy[5].
  • Infantile convulsions and choreoathetosis's MeSH descriptor ID is recorded as C535522[6].
  • Infantile convulsions and choreoathetosis's OMIM ID is recorded as 602066[7].
  • Infantile convulsions and choreoathetosis's Orphanet ID is recorded as 31709[8].
  • Infantile convulsions and choreoathetosis's NCI Thesaurus ID is recorded as C126650[9].
  • Infantile convulsions and choreoathetosis's genetic association is recorded as PRRT2[10].
  • Infantile convulsions and choreoathetosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_31709[11].
  • Infantile convulsions and choreoathetosis's UMLS CUI is recorded as C1865926[12].
  • Infantile convulsions and choreoathetosis's ICD-10-CM is recorded as G40.4[13].
  • Infantile convulsions and choreoathetosis's GARD rare disease ID is recorded as 8553[14].
  • Infantile convulsions and choreoathetosis's Mondo ID is recorded as MONDO_0011178[15].
  • Infantile convulsions and choreoathetosis's Microsoft Academic ID is recorded as 2777071988[16].
  • Infantile convulsions and choreoathetosis's Microsoft Academic ID is recorded as 2909025762[17].
  • Infantile convulsions and choreoathetosis's UniProt disease ID is recorded as DI-03372[18].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [9] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [10] ↑ . Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [13] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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