Ehlers-Danlos syndrome, arthrochalasia type https://rarediseases.info.nih.gov/diseases/2084/arthrochalasia-ehlers-danlos-syndrome https://www.malacards.org/card/ehlers_danlos_syndrome_arthrochalasia_type_1 https://www.malacards.org/card/ehlers_danlos_syndrome_arthrochalasia_type_3 Ehlers-Danlos syndrome, arthrochalasia type, 1 Ehlers-Danlos syndrome type 7 EDS VII Ehlers-Danlos syndrome type 7A (formerly) An inherited connective tissue disorder that is caused by defects in a protein called collagen. Common symptoms include severe joint hypermobility ; congenital hip dislocation; fragile, hyperextensible skin; hypotonia ; and kyphoscoliosis (kyphosis and scoliosis). EDS, arthrochalasia type is caused by changes (mutations) in the COL1A1 gene or the COL1A2 gene and is inherited in an autosomal dominant manner. Treatment and management is focused on preventing serious complications and relieving associated signs and symptoms. SCTID:4170004 EDS7A (formerly) MEDGEN:1645042 EDSARTH1 NANDO:1200650 NANDO:2201260 Orphanet:1899 arthrochalasis multiplex congenita UMLS:C4551623 Ehlers-Danlos syndrome, type VII, autosomal dominant GARD:0002084 DOID:0080727 arthrochalasia EDS AEDS arthrochalasia Ehlers-Danlos syndrome Ehlers-Danlos syndrome, type VIIA, autosomal dominant MONDO:0007525 EDS 7A EDS 7B EDS VII, mutant procollagen type MESH:C562625 NCIT:C125701 Ehlers-Danlos syndrome, type VII Ehlers-Danlos syndrome, arthrochalasia type Ehlers-Danlos syndrome