vascular disorder autosomal recessive disease autosomal recessive cutis laxa type 1 https://github.com/monarch-initiative/mondo/issues/5663 https://www.malacards.org/card/autosomal_recessive_cutis_laxa_type_i Orphanet:90349 GARD:0008480 SCTID:254222002 cutis laxa, type 1 MESH:C536225 MONDO:0019572 Autosomal recessive cutis laxa, type 1 (ARCL1) is a generalized connective tissue disorder characterized by the association of wrinkled, redundant and sagging inelastic skin with severe systemic manifestations (lung atelectesias and emphysema, vascular anomalies, and gastrointestinal and genitourinary tract diverticuli). autosomal recessive cutis laxa type 1 autosomal recessive cutis laxa with severe systemic involvement MEDGEN:78663 PMID:19401719 ARCL1 DOID:0070144 autosomal recessive cutis laxa, pulmonary emphysema type UMLS:C0268351 cutis laxa, autosomal recessive type 1 inherited cutis laxa