syndromic disease intestinal disorder aplasia cutis congenita-intestinal lymphangiectasia syndrome https://github.com/monarch-initiative/mondo/issues/6878 https://www.malacards.org/card/aplasia_cutis_congenita_with_intestinal_lymphangiectasia Aplasia cutis congenita - intestinal lymphangiectasia is an extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterized by aplasia cutis congenita of the vertex and generalized edema (as well as hypoproteinemia and lymphopenia) due to intestinal lymphangiectasia. There have been no further descriptions in the literature since 1985. OMIM:207731 autosomal recessive aplasia cutis MONDO:0008808 MESH:C537788 aplasia cutis congenita intestinal lymphangiectasia SCTID:720500008 GARD:0000753 UMLS:C1859753 Bronspiegel-Zelnick syndrome MEDGEN:349241 Orphanet:1116 primary lymphedema mixed dermis disorder