syndromic disease hereditary disease obsolete dermis elastic tissue disorder developmental defect during embryogenesis Ehlers-Danlos syndrome https://github.com/monarch-initiative/mondo/issues/5682 https://www.malacards.org/card/ehlers_danlos_syndrome MESH:D004535 Danlos Disease, Ehlers Meekeren-Ehlers-Danlos syndrome Disease, Ehlers Danlos SCTID:398114001 Ehlers Danlos Syndrome Orphanet:98249 Danlos disease Disease, Ehlers-Danlos Fibrodysplasia elastica generalisata Ehlers-Danlos syndromes ED syndrome NANDO:2200607 MEDGEN:41720 DOID:13359 elastic skin MedDRA:10014316 NORD:1080 Hereditary collagen dysplasia skin elastic Ehlers-Danlos Disease icd11.foundation:1122707206 danlos ehlers syndrome MONDO:0020066 NCIT:C34568 UMLS:C0013720 Ehlers Danlos Disease EDS ICD10CM:Q79.6 OMIMPS:130000 Ehler Danlos Syndrome Syndrome, Ehlers-Danlos NANDO:1200645 GARD:0006322 Ehlers Danlos syndrome Dystrophia mesodermalis congenita ICD9:756.83 The Ehlers–Danlos syndromes (EDS) are a clinically and genetically heterogeneous group of heritable connective tissue disorders (HCTDs) characterized by joint hypermobility, skin hyperextensibility, and tissue fragility. hereditary disorder of connective tissue