Item 6 of 30 (back to results) previous next   Nablus mask-like facial syndrome C536110               MeSH Unique Identifier: C536110 Scope Notes: Upswept frontal hairline, tight glistening facial skin, high-arched and sparse eyebrows, absent/scant eyelashes, hypertelorism, blepharophimosis Click here for more information

Current search: C11. Eye Diseases: Eye Diseases [MESH:D005128] > Eyelid Diseases [MESH:D005141] > Blepharophimosis [MESH:D016569] × 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)   Musculoskeletal Abnormalities [MESH:D009139] (3796)   Craniofacial Abnormalities [MESH:D019465] (3098)   Nablus mask-like facial syndrome [MESH:C536110] (1) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Eye Abnormalities [MESH:D005124] (1233)   Blepharophimosis [MESH:D016569] (30)   Nablus mask-like facial syndrome [MESH:C536110] (1)  Eyelid Diseases [MESH:D005141] (882)   Blepharophimosis [MESH:D016569] (30)   Nablus mask-like facial syndrome [MESH:C536110] (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)   Nablus mask-like facial syndrome [MESH:C536110] (1)  Eye Abnormalities [MESH:D005124] (1233)   Blepharophimosis [MESH:D016569] (30)   Nablus mask-like facial syndrome [MESH:C536110] (1)  Musculoskeletal Abnormalities [MESH:D009139] (3779)   Craniofacial Abnormalities [MESH:D019465] (3064)   Nablus mask-like facial syndrome [MESH:C536110] (1)