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Noonan syndrome 3

Go to external page http://purl.obolibrary.org/obo/MONDO_0012371

Any Noonan syndrome in which the cause of the disease is a mutation in the KRAS gene. [ MONDO:patterns/disease_series_by_gene ]

Synonyms: Noonan syndrome type 3 KRAS Noonan syndrome Noonan syndrome 3 KRAS gene related Noonan syndrome Noonan syndrome caused by mutation in KRAS NS3

This is just here as a test because I lose it

Term information

database cross reference
  • DOID:0060581 (MONDO:equivalentTo)
  • UMLS:C1860991 (MONDO:equivalentTo)
  • NCIT:C176931 (MONDO:equivalentTo)
  • GARD:9885 (MONDO:GARD)
  • OMIM:609942 (MONDO:equivalentTo)
  • MESH:C537847 (MONDO:equivalentTo)
  • MEDGEN:349931 (MONDO:equivalentTo)
Subsets

gard_rare, rare, nord_rare

exactMatch

http://identifiers.org/mesh/C537847

http://purl.obolibrary.org/obo/NCIT_C176931

http://purl.obolibrary.org/obo/DOID_0060581

https://omim.org/entry/609942

http://identifiers.org/medgen/349931

http://linkedlifedata.com/resource/umls/id/C1860991

id

MONDO:0012371

seeAlso

https://rarediseases.info.nih.gov/diseases/9885/noonan-syndrome-3