diff --git a/modules/Sample/Diagnosis.yaml b/modules/Sample/Diagnosis.yaml
index f1878a5f..4376c837 100644
--- a/modules/Sample/Diagnosis.yaml
+++ b/modules/Sample/Diagnosis.yaml
@@ -12,7 +12,7 @@ enums:
       #  meaning: https://www.ebi.ac.uk/ols/ontologies/cco/terms?iri=http%3A%2F%2Fidentifiers.org%2Fomim%2F101000
       Schwannomatosis:
         description: A rare genetic disorder characterized by the presence of multiple schwannomas.
-        meaning: https://www.ebi.ac.uk/ols/ontologies/ncit/terms?iri=http%3A%2F%2Fpurl.obolibrary.org%2Fobo%2FNCIT_C6557
+        meaning: http://purl.obolibrary.org/obo/NCIT_C6557
       NF2-related schwannomatosis:
         description: Previously known as Neurofibromatosis type 2.
       SMARCB1-related schwannomatosis:
@@ -26,6 +26,9 @@ enums:
           Most schwannomas originate from the eighth cranial nerve, whereas neurofibromas more commonly arise along the spinal nerve roots.
         notes:
         - Not in NCIT as of 2023-06-07
+      Noonan Syndrome: 
+        description: A rare, highly variable, multisystemic disorder mainly characterized by short stature, distinctive facial features, congenital heart defects, cardiomyopathy and an increased risk to develop tumors in childhood.
+        meaning: http://www.orpha.net/ORDO/Orphanet_648
       Not Applicable:
   
   AgeGroupEnum: