Hemoglobin H disease Hemoglobin H disease also known as Alpha thalassemia intermedia that is caused by deletion of three alpha-globin genes (only one normal alpha gene
Acute intermittent porphyria Acute intermittent porphyria also called "AIP" or Swedish Porphyria is one of the acute porphyrias, which are a group of rare inherited metabolic
What is tyrosinemia Tyrosinemia also called hereditary tyrosinemia, refers to a group of genetic disorders characterized by disruptions in the multistep process that breaks down
Primary biliary cirrhosis Primary biliary cirrhosis is now known as primary biliary cholangitis or PBC is a chronic progressive autoimmune liver disease in which the small bile
What is CREST syndrome CREST syndrome is now called limited scleroderma, is a widespread connective tissue disease characterized by changes in the skin, blood vessels,
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
What is mycetoma Mycetoma is a chronic, granulomatous, subcutaneous, inflammatory disease caused by true fungi (eumycetoma) or filamentous bacteria (actinomycetoma, bacteria that produce filaments, like
Bartonellosis Bartonellosis is a group of infectious diseases in both animals and humans caused by Bartonella bacteria with Bartonella henselae (cat scratch disease), Bartonella bacilliformis
Lymphogranuloma venereum Lymphogranuloma venereum is an ulcerative disease of the genital area that is caused by the gram-negative bacteria Chlamydia trachomatis, especially serovars L1, L2,