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more general categories information about this item C15. Hemic and Lymphatic Diseases C15. Hemic and Lymphatic Diseases Lymphatic Diseases [MESH:D008206] (5167) Lymphangiectasis [MESH:D008200] (20) Lymphangiectasis, Intestinal [MESH:D008201] (18) Aplasia cutis congenita intestinal lymphangiectasia [MESH:C537788] (1) Lymphatic Abnormalities [MESH:D044148] (251) Lymphangiectasis, Intestinal [MESH:D008201] (18) Aplasia cutis congenita intestinal lymphangiectasia [MESH:C537788] (1) C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152) Congenital Abnormalities [MESH:D000013] (8109) Abnormalities, Multiple [MESH:D000015] (3192) Ectodermal Dysplasia [MESH:D004476] (938) Aplasia cutis congenita intestinal lymphangiectasia [MESH:C537788] (1) Lymphatic Abnormalities [MESH:D044148] (251) Lymphangiectasis, Intestinal [MESH:D008201] (18) Aplasia cutis congenita intestinal lymphangiectasia [MESH:C537788] (1) Skin Abnormalities [MESH:D012868] (1723) Ectodermal Dysplasia [MESH:D004476] (958) Aplasia cutis congenita intestinal lymphangiectasia [MESH:C537788] (1) Genetic Diseases, Inborn [MESH:D030342] (9766) Skin Diseases, Genetic [MESH:D012873] (3456) Ectodermal Dysplasia [MESH:D004476] (958) Aplasia cutis congenita intestinal lymphangiectasia [MESH:C537788] (1) C17. Skin and Connective Tissue Diseases C17. Skin and Connective Tissue Diseases Skin Diseases [MESH:D012871] (8774) Skin Abnormalities [MESH:D012868] (1709) Ectodermal Dysplasia [MESH:D004476] (958) Aplasia cutis congenita intestinal lymphangiectasia [MESH:C537788] (1) Skin Diseases, Genetic [MESH:D012873] (3481) Ectodermal Dysplasia [MESH:D004476] (958) Aplasia cutis congenita intestinal lymphangiectasia [MESH:C537788] (1)
