has characteristic has characteristic has material basis in germline mutation in LTBP4 Autosomal recessive inheritance autosomal recessive disease cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies https://www.malacards.org/card/cutis_laxa_autosomal_recessive_type_ic cutis laxa with Severe pulmonary, gastrointestinal, and urinary abnormalities MESH:C567716 ARCL1C PMID:19836010 GARD:0017140 MEDGEN:442566 OMIM:613177 icd11.foundation:424903269 autosomal recessive cutis laxa type IC Urban-Rifkin-Davis syndrome DOID:0070139 autosomal recessive cutis laxa type 1C MONDO:0013170 UMLS:C2750804 cutis laxa, autosomal recessive, type IC A autosomal recessive cutis laxa type I that has material basis in homozygous or compound heterozygous mutation in the LTBP4 gene on chromosome 19q13 cutis laxa, autosomal recessive, type 1C Orphanet:221145 inherited cutis laxa