Disease Index

melanocytic nevus that involves the skin of eyelid

human disease

neoplasm (disease) that involves the sebaceous gland of eyelid

human disease

human disease

endocrine system disease that is located in the pancreas

disease

human disease

endocrine gland cancer located in the pancreas

human disease

Human disease

This syndrome is characterized by exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis

Human disease

Human disease

autosomal recessive disorder caused by mutation(s) in the PNLIP gene, encoding pancreatic triacylglycerol lipase. The condition is characterized by absent or reduced pancreatic lipase

Human disease

human disease

human disease

hypothesis that there exists a subset of children with rapid onset of obsessive-compulsive disorder or tic disorders and these symptoms are caused by group A beta-hemolytic streptococcal infections

human disease

human disease

medical condition

human disease

neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the PANK2 gene on chromosome 20p13

Human disease

Pyogenic arthritis-pyoderma gangrenosum-acne syndrome is a rare pleiotropic autoinflammatory disorder of childhood, primarily affecting the joints and skin

papillary carcinoma that involves the uterine cervix

papillary carcinoma that involves the body of uterus

cancerous tumor