syndromic disease hereditary disease vascular disorder angioosteohypertrophic syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/5682 https://github.com/monarch-initiative/mondo/issues/6740 https://github.com/monarch-initiative/mondo/issues/6751 https://github.com/monarch-initiative/mondo/issues/6877 https://rarediseases.info.nih.gov/diseases/3122/klippel-trenaunay-syndrome https://www.malacards.org/card/klippel_trenaunay_weber_syndrome Klippel-Trenaunay-Weber syndrome, Isolated cases NORD:1337 Klippel-Trénaunay-Weber syndrome Klippel-Trenaunay syndrome Klippel-Trenaunay-Weber syndrome NANDO:2201030 Klippel-Trenaunay Syndrome MedDRA:10051452 SCTID:721105004 angio-osteohypertrophy syndrome Orphanet:90308 MESH:D007715 DOID:2926 haemangiectatic hypertrophy MONDO:0007864 OMIM:149000 Orphanet:2346 Klippel-Trénaunay syndrome KTS NCIT:C84801 Weber-Klippel-Trenaunay Klippel Trenaunay syndrome icd11.foundation:1561120378 NANDO:1200884 A congenital vascular bone syndrome (CVBS) characterized by the presence of a vascular malformation in a limb, mainly of the arteriovenous type, which results in overgrowth of the affected limb. GARD:0003122 MEDGEN:9646 angioosteohypertrophy syndrome UMLS:C0022739 skin vascular disease overgrowth syndrome developmental defect during embryogenesis