Item 1 of 1 (back to results)   Catel Manzke syndrome C535347

Current search: C05. Musculoskeletal Diseases: Musculoskeletal Diseases [MESH:D009140] > Jaw Diseases [MESH:D007571] > Jaw Abnormalities [MESH:D007569] > Pierre Robin Syndrome [MESH:D010855] > Catel Manzke syndrome [MESH:C535347] × Select any link to see items in a related category. more general categories    information about this item C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Hand Deformities [MESH:D006226] (590)   Hand Deformities, Congenital [MESH:D006228] (587)   Catel Manzke syndrome [MESH:C535347] (1)  Jaw Diseases [MESH:D007571] (1601)   Jaw Abnormalities [MESH:D007569] (1435)   Pierre Robin Syndrome [MESH:D010855] (101)   Catel Manzke syndrome [MESH:C535347] (1)  Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Pierre Robin Syndrome [MESH:D010855] (101)   Catel Manzke syndrome [MESH:C535347] (1)  Limb Deformities, Congenital [MESH:D017880] (1813)   Upper Extremity Deformities, Congenital [MESH:D038062] (604)   Hand Deformities, Congenital [MESH:D006228] (587)   Catel Manzke syndrome [MESH:C535347] (1) C07. Stomatognathic Diseases  C07. Stomatognathic Diseases  Stomatognathic Diseases [MESH:D009057] (5348)   Jaw Diseases [MESH:D007571] (1608)   Jaw Abnormalities [MESH:D007569] (1435)   Pierre Robin Syndrome [MESH:D010855] (101)   Catel Manzke syndrome [MESH:C535347] (1)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Pierre Robin Syndrome [MESH:D010855] (101)   Catel Manzke syndrome [MESH:C535347] (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)   Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Maxillofacial Abnormalities [MESH:D019767] (1448)   Jaw Abnormalities [MESH:D007569] (1435)   Pierre Robin Syndrome [MESH:D010855] (101)   Catel Manzke syndrome [MESH:C535347] (1)  Limb Deformities, Congenital [MESH:D017880] (1813)   Hand Deformities, Congenital [MESH:D006228] (587)   Catel Manzke syndrome [MESH:C535347] (1)  Stomatognathic System Abnormalities [MESH:D018640] (1705)   Maxillofacial Abnormalities [MESH:D019767] (1447)   Jaw Abnormalities [MESH:D007569] (1438)   Pierre Robin Syndrome [MESH:D010855] (101)   Catel Manzke syndrome [MESH:C535347] (1)