Disease Index

congenital nervous system abnormality characterized by migration of neurons to ectopic locations in the brain where the neurons form areas that appear as band-like clusters of white tissue underneath the gray tissue of the cerebral cortex

Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare cytotoxic cutaneous lymphoma that has been recognized as a distinct subset of peripheral T-cell lymphomas originating and presenting primarily in the subcutaneous fat tissue

disease involving the superficial fascia

low-grade astrocytic brain tumor (astrocytoma) that arises within the ventricles of the brain

human disease

human disease

Human disease

human disease

human disease

human disease

Rare disorder involving deficiency in GABA degradation

Succinyl-CoA:3-ketoacid CoA transferase deficiency (SCOTD) is a defect in ketone body utilization characterized by severe, potentially fatal intermittent episodes of ketoacidosis

Congenital sucrase-isomaltase deficiency (CSID) is a carbohydrate intolerance disorder characterised by malabsorption of oligosaccharides and disaccharides

Sudden infant death with dysgenesis of the testes (SIDDT) syndrome is a lethal condition in infants with dysgenesis of testes

Human disease

brachydactyly characterized by a nonarticulating great toe set dorsal and proximal to the typical position

human disease

Human disease

poorly circumscribed, intermediate fibrocytic neoplasm arising from the superficial soft tissues

medical condition

thinning or erosion of the bony layer covering the superior semicircular canal, causing abnormal exposure of the vestibular membranous labyrinth to the middle cranial fossa

ocular disease characterized by episodes of recurrent inflammation of the superior cornea and limbus, as well as of the superior tarsal and bulbar conjunctiva

form of epidermolysis bullosa simplex in which blistering occurs above the basal keratinocytes

oculomotor palsy that arises from lesions in the supranuclear pathways controlling extraocular movement

human disease

Human disease

human disease