Solitary thyroid nodule Thyroid nodule is a discrete lesion or abnormal growth of thyroid cells that forms a lump within the thyroid gland that can be

Fulminant hepatic failure Fulminant hepatic failure also known as acute liver failure, is usually defined as the development of severe acute liver injury or severe

Pseudohypoaldosteronism Pseudohypoaldosteronism comprises a heterogeneous group of disorders of electrolyte metabolism characterized by an apparent state of renal tubular unresponsiveness or resistance to the action

Hypophosphatemic rickets Hypophosphatemic rickets also known as vitamin D-resistant rickets, hereditary hypophosphatemic rickets or familial hypophosphatemic rickets, is an inherited disorder related to low levels of

Constitutional growth delay Constitutional growth delay also called constitutional delay of growth and puberty, is a variant of normal growth rather than a disorder. Children with

Congenital hepatic fibrosis Congenital hepatic fibrosis is an inherited disease of the liver that is present from birth. Congenital hepatic fibrosis is characterized by malformation

Congenital hyperinsulinism Congenital hyperinsulinism also called familial hyperinsulinism, persistent hyperinsulinemic hypoglycemia of infancy, infancy hyperinsulinemia hypoglycemia or islet cell dysregulation syndrome, is a rare genetic disorder that

Adrenal hypoplasia Adrenal hypoplasia is a condition in which there is underdevelopment or hypotrophy of the adrenal cortex due to several clinical conditions. Adrenal hypoplasia

Triple A syndrome Triple A syndrome also called "AAA syndrome", Achalasia-Addisonianism-Alacrima syndrome or Allgrove syndrome, is an inherited condition characterized by three specific features: achalasia, Addison

Kostmann syndrome Kostmann syndrome also called "severe congenital neutropenia", Kostmann disease, Kostmann neutropenia, genetic infantile agranulocytosis or infantile genetic agranulocytosis, is a rare inherited disorder