syndromic developmental defect of the eye syndromic urogenital tract malformation polymalformative genetic syndrome with increased risk of developing cancer Noonan syndrome DOID:3490 GARD:0010955 ICD10:Q87.1 ICD9:759.89 MESH:D009634 MONDO:0018997 MedDRA:10029748 NCIT:C34854 Noonan Syndrome (NS) is characterised by short stature, typical facial dysmorphism and congenital heart defects. Noonan syndrome Noonan's syndrome Noonan-Ehmke syndrome OMIMPS:163950 Orphanet:648 SCTID:205824006 Turner's phenotype, karyotype normal UMLS:C0028326 Ullrich-Noonan syndrome pseudo-Ullrich-Turner syndrome hereditary lymphedema syndromic lymphedema syndromic renal or urinary tract malformation malposition of external canthus rare disorder with ptosis Noonan syndrome and Noonan-related syndrome RASopathy genetic multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome neurovascular disease