Directory
Homocystinuria due to MTHFR deficiency
Homocystinuria associated with methylenetetrahydrofolate reductase (MTHFR) deficiency is a rare inherited disorder that is caused by...
Human granulocytic ehrlichiosis
Human granulocytic ehrlichiosis is an infectious disease caused by bacteria of the genus Ehrlichia, transmitted through tick bites...
H1N1 flu
H1N1 influenza, also known as swine flu, is an infectious disease caused by the influenza A(H1N1) virus. This virus...
Hernia
A hernia is a pathology characterized by the protrusion of an organ or part of it through a pathological gap in the wall of the cavity where...
Herniated disc
A herniated disc is a common condition in which a disc located between the vertebrae bulges outward.
Hiatal hernia
A hiatal hernia (HH) is a condition in which part of the stomach or other organs ...
High molecular weight kininogen deficiency
High molecular weight kininogen deficiency (HMWK) is a rare inherited disorder that results from inadequate production of the kininogen...
Holocarboxylase synthetase deficiency
Holocarboxylase synthetase (HCS) deficiency is a rare inherited disorder associated with impaired synthesis of an important enzyme,...
Prenatal herpes virus infection
Prenatal herpes virus infection is one of the most common infections affecting women during pregnancy. The most common...
His fascicular tachycardia
Fascicular tachycardia (fascicular reciprocal) is a type of paroxysmal tachycardia that is caused by repetitive...
Heartburn
Heartburn is an unpleasant burning sensation in the chest and throat caused by the reflux of stomach acid into the esophagus.
Hiccups
Hiccups are brief, sudden, and involuntary contractions of the diaphragm that produce a characteristic sound...
Helicobacter Pylori Infection
Helicobacter pylori (H. pylori) infection is a gastrointestinal disorder caused by a spiral-shaped, gram-negative bacterium, ...
Hookworm infection
Ancylostomiasis is a helminthic disease caused by parasites of the genus Ancylostoma, such as Ancylostoma duodenale and Necator amer...
Human papillomavirus infection
Human papillomavirus (HPV) is a group of more than 150 different types of viruses that can infect epithelial tissues...
Hantavirus infection
Hantavirus infection is an acute infectious disease caused by viruses of the Bunyaviridae family, which have zoonotic...
Hypochondria
Hypochondria, according to medical literature, is a mental disorder characterized by excessive preoccupation with...
Harlequin Ichthyosis
Harlequin ichthyosis, or isolated ichthyosis dysplasia, is a rare genetic disorder characterized by an extr...
Liver ischemia
Liver ischemia is a condition characterized by insufficient blood supply to the liver, which can lead to impaired liver function.
Cystic hamartoma of the liver
Cystic hamartoma of the liver (CHL) is a rare benign tumor characterized by cystic transformation of the he...
Hodgkin's lymphoma
Hodgkin's lymphoma (HL) is a type of lymphoma, which is a malignant tumor of the lymphatic system. It is a disease that occurs in the l...
HTLV-1 associated myelopathy
HTLV-1 (human T-lymphotropic virus type 1)-associated myelopathy is a progressive disease associated with...
Hammer toe deformity
Hammer toe, also known as mallet toe, is a morphological change characterized by...
Human monocytic ehrlichiosis
Human monocytic ehrlichiosis is an infectious disease caused by a bacterial infection caused by Ehrlichia. These microorganisms are...
Hereditary alpha-tryptasemia
Hereditary alpha-tryptasemia (HAT) is a rare genetic disorder caused by a defect in the metabolism of the protein alpha-tryptase...
Hereditary ataxia
Hereditary ataxia is a group of neurodegenerative diseases characterized by progressive loss of coordination...
Hereditary hemorrhagic telangiectasia
Hereditary hemorrhagic telangiectasia (HHT), also known as Osler-Weber-Rendu disease, is an inherited...
Hereditary hyperekplexia
Hereditary hyperekplexia is a rare neurological disorder characterized by increased reactivity of reflexes, which leads to...
Hereditary coproporphyria
Hereditary coproporphyria (HC) is a rare genetic disorder belonging to the group of porphyrias, characterized by...
Hereditary xanthinuria
Hereditary xanthinuria is a rare genetic disorder associated with a disorder of purine metabolism and characterized by increased ...
