Noonan syndrome 7

Noonan syndrome that has material basis in heterozygous mutation in the BRAF gene
MedicalCondition rare_disease Q26492795
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Noonan syndrome 7

Summary

Noonan syndrome 7 is a rare disease[1].

Key Facts

  • Noonan syndrome 7's instance of is recorded as rare disease[2].
  • Noonan syndrome 7's subclass of is recorded as Noonan syndrome[3].
  • Noonan syndrome 7's OMIM ID is recorded as 613706[4].
  • Noonan syndrome 7's genetic association is recorded as BRAF[5].
  • Noonan syndrome 7's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_648[6].
  • Noonan syndrome 7's UMLS CUI is recorded as C3150970[7].
  • Noonan syndrome 7's ICD-10-CM is recorded as Q87.1[8].
  • Noonan syndrome 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[9].
  • Noonan syndrome 7's Mondo ID is recorded as MONDO_0013379[10].
  • Noonan syndrome 7's UniProt disease ID is recorded as DI-02990[11].

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APA 4ort.xyz Knowledge Graph. (2026). Noonan syndrome 7. Retrieved May 3, 2026, from https://4ort.xyz/entity/noonan-syndrome-7
MLA “Noonan syndrome 7.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/noonan-syndrome-7.
BibTeX @misc{4ortxyz_noonan-syndrome-7_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Noonan syndrome 7}}, year = {2026}, url = {https://4ort.xyz/entity/noonan-syndrome-7}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Noonan syndrome 7 — https://4ort.xyz/entity/noonan-syndrome-7 (retrieved 2026-05-03)

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