Directory
Hereditary methemoglobinemia
Hereditary methemoglobinemia is a rare genetic disorder characterized by impaired oxygen transport in the body and...
Hereditary mucoepithelial dysplasia
Hereditary mucoepithelial dysplasia (HMD) is a rare genetic disorder characterized by atypical development of...
Hereditary neuralgic amyotrophy
Hereditary neuralgic amyotrophy (HNA), also known as amytrophic lateral sclerosis (ALS) or Stevens disease, is a...
Hereditary neuroblastoma
Hereditary neuroblastoma is a malignant tumor that originates from primitive neuroblasts, which are cells responsible for...
Hereditary fructose intolerance
Hereditary fructose intolerance (HFI) is a rare but serious metabolic disorder associated with the absence or de...
Hereditary retinoblastoma
Hereditary retinoblastoma (RB) is a malignant tumor that originates from the cells of the retina of the eye and predominantly affects the retinal...
Hereditary sensory and autonomic neuropathy type 2
Hereditary sensory and autonomic neuropathy type 2 (HSAN II) is a rare genetic disorder characterized by...
Hereditary sensory neuropathy type 1 (HSN1)
Hereditary sensory neuropathy type 1 (HSN1) is a rare inherited disorder that is caused by degenerative changes in the...
Hereditary resistance to antivitamin K
Hereditary antivitamin K resistance is a rare inherited disorder associated with a metabolic disorder in...
Hereditary cerebral amyloid angiopathy
Hereditary cerebral amyloid angiopathy (HCAA) is a disease characterized by the deposition of amyloid protein in the wall of the...
Hereditary multiple osteochondromas
Hereditary multiple osteochondroma (HMO) is a rare inherited disorder characterized by the formation of benign tumors...
Hereditary angioedema
Hereditary angioedema (HAE) is a rare genetic disorder characterized by episodes of sudden and extensive ...
Hereditary keratitis
Hereditary keratitis is a rare hereditary disease characterized by damage to the cornea of the eye. This pathological...
Hereditary ovalocytosis
Hereditary ovalocytosis is a rare genetic disorder that belongs to a group of hereditary anemias and is characterized by altered...
Hereditary pancreatitis
Hereditary pancreatitis (HP) is a chronic inflammatory disease of the pancreas that has a genetic predisposition...
Hereditary pyropoikilocytosis
Hereditary pyropoikilocytosis is a rare genetic blood disorder associated with an abnormality in the extraction of hemoglobin from red blood cells...
Hereditary paraganglioma-pheochromocytoma syndrome
Paragangliomas and pheochromocytomas are rare tumors that arise from chromaffin cells, which are responsible for synthesizing and secreting...
Hereditary spastic paraparesis
Hereditary spastic paraparesis (HSP) is a group of neurological diseases characterized by progressive...
Hereditary spherocytosis
Hereditary spherocytosis is a genetically determined disease characterized by a change in the shape of red blood cells - cl...
Hereditary elliptocytosis
Hereditary elliptocytosis is a genetic disorder characterized by a change in the shape of red blood cells to ellipsoid, ...
Hypothalamic tumor
A hypothalamic tumor is a rare neoplasm that occurs in the hypothalamus, a brain structure responsible for regulating many...
Heart tumor
A cardiac tumor is a rare neoplasm that occurs in or on the surface of the heart tissue. These tumors can be...
Acute cardiovascular disease
Acute cardiovascular disease (ACD) is a group of diseases that occur against the background of acute circulatory failure...
Heavy metal poisoning
Heavy metal poisoning is a group of different medical conditions that result from exposure to current...
Pediculosis
Pediculosis, or infestation with head, body, or pubic lice, is a transmissible skin disease caused by ...
Perstans lenticular hyperkeratosis
Perstans lenticular hyperkeratosis (PLK) is a rare chronic skin disease belonging to the group of dysostoses, characterized by...
Hepatic veno-occlusive disease with immunodeficiency
Hepatic veno-occlusive disease (HVOD) is a rare pathological condition characterized by occlusion of the hepatic veins and/or their c...
Head and neck squamous cell carcinoma (HNSCC)
Head and neck squamous cell carcinoma (HNSCC) is an aggressive malignancy that develops from squamous cell...
Horseshoe kidney
A horseshoe kidney is an anatomical anomaly that is the fusion of both kidneys at the bottom, resulting in the formation of...
Hearing loss
Hearing loss is a reduction in the ability to detect sound waves, which can significantly reduce quality of life. It can manifest itself in ...
