Directory
Tuberculous meningitis
Tuberculous meningitis is a rare but extremely serious form of meningitis caused by infection with mycobacteria...
Tuberculous uveitis
Tuberculous uveitis is an inflammation of the vascular tunic of the eye caused by infection with Mycobacterium tuberculosis. It is a rare...
Tuberous sclerosis
Tuberous sclerosis (TS) is a hereditary disease characterized by the formation of benign tumors (tubers) in different...
Tubular aggregate myopathy
Tubular aggregated myopathy (TAM) is a rare inherited disorder that involves abnormal myofibrillar structure...
Tularemia
Tularemia is an acute infectious disease caused by the bacteria Francisella tularensis, a member of the genus Francisella. These microbes...
Tumfectious multiple sclerosis
Tumultuous multiple sclerosis (TMS) is a complex neurodegenerative disease that affects the central nervous system...
Tungiasis
Tungiasis is a disease caused by an infection caused by mites belonging to the genus Tunga. These parasites penetrate the skin of humans, ...
Thyroid nodule
A thyroid nodule is a localized growth in the thyroid tissue that can be either benign or malignant.
Trichoclasis nodosa
Trichoclasis nodosa is a disorder characterized by the presence of nodules in the hair caused by abnormalities in its structural components...
Testicular compaction
Testicular hardening is a pathological condition characterized by a change in the texture or density of the tissue of one or both testicles.
Traumatic brain injury
Traumatic brain injury (TBI) is damage to the brain and/or skull caused by external damaging factors, such as...
Testicular failure
Testicular failure (or testicular insufficiency) is a condition in which the testicles do not produce enough ...
Arterial trunk
Truncus arteriosus is a rare but serious condition characterized by abnormal development of the main arteries of the heart, which results in...
Toxocariasis
Toxocariasis is a zoonotic infectious disease caused by parasites of the genus Toxocara, most commonly Toxocara canis and Toxocara cati, which...
Toxoplasmosis
Toxoplasmosis, caused by the protozoan parasite Toxoplasma gondii, is a zoonotic infectious disease that affects...
Triploidy
Triploidy is a chromosomal disorder characterized by the presence of a triple set of chromosomes (69 chromosomes instead of the normal 46). This is a...
Trichomoniasis
Trichomoniasis is an infectious disease caused by the parasite Trichomonas vaginalis, which most often affects the genitourinary organs of humans...
Trichothiodystrophy
Trichothiodystrophy (TTD) is a rare genetic disorder that causes severe disturbances in the structure and function of hair, skin...
Trichoepithelioma
Trichoepithelioma is a rare benign tumor formation characterized by the appearance of single or multiple nodes...
VIPoma
VIPoma, also known as vasoactive intestinal polyp, is a rare endocrine neoplastic process that usually...
X-linked agammaglobulinemia
X-linked agammaglobulinemia is a rare inherited immunodeficiency disorder characterized by...
Vaginal agenesis
Vaginal agenesis (vaginal aplasia) is a rare genetic disorder characterized by the absence or underdevelopment of the vaginal...
Aneurysm of the vein of Galen
Aneurysm of the vein of Galen is a developmental anomaly characterized by an increase in the venous space in the region of the vein of Galen, which...
Anemia due to vitamin B12 deficiency
Vitamin B12 deficiency anemia is a condition characterized by low levels of red blood cells in the...
Watermelon stomach
Watermelon stomach, or axial gastroptosis, is a condition in which the stomach descends into the abdominal cavity below its ...
VACTERL Association
VACTERL association is a non-genetic syndrome characterized by clusters of congenital anomalies in multiple organs and ...
White spongy nevus
White spongy nevus (fungiform nevus) is a benign neoplasm characterized by increased proliferation...
Y-chromosome infertility
Y-chromosome infertility is one of the serious genetic diseases that can lead to male infertility as a result of...
Wandering spleen
Floating spleen, or splenomegaly of uncertain location, is a clinical condition characterized by an anoma...
Von Willebrand disease (VWD)
Von Willebrand disease (VWD) is an inherited disorder of hemostasis that is caused by deficiency or dysfunction of the von Willebrand factor...
