Directory
Wilms tumor syndromes associated with WT1
Wilms tumor syndromes (Wilms syndrome) are rare malignant neoplasms of the kidney characterized by the formation of...
Vascular dementia
Vascular dementia is one of the most common types of cognitive impairment in older adults. It occurs due to...
Vascular ring
A vascular ring is an anomaly of the aortic structure characterized by the presence of additional vascular elements that can lead to...
Vascular birthmark
A vascular birthmark is a benign vascular lesion on the skin that results from abnormal growth of capillaries...
Vascular Ehlers-Danlos syndrome (VEDS)
Vascular Ehlers-Danlos syndrome (VEDS) is an inherited connective tissue disorder characterized by an...
Urethral stricture
Urethral stricture is a condition characterized by narrowing of the urethra, which leads to difficulty urinating and various associated...
X-linked spinal muscular atrophy in children
Childhood spinal muscular atrophy (SMA) is a group of genetically determined disorders characterized by the loss of motor neurons...
X-linked mental retardation, Siderius type
X-linked mental retardation, Siderius type, is a genetic disorder characterized by impaired...
X-linked juvenile retinoschisis
Juvenile retinoschisis is an inherited disorder of the retina that is transmitted on the X chromosome and primarily affects the...
ZAP70-associated severe combined immunodeficiency
ZAP70-associated severe combined immunodeficiency is a rare genetic disorder characterized by abnormal...
X-linked severe combined immunodeficiency
X-linked severe combined immunodeficiency (X-linked SCID) is a rare inherited disorder characterized by...
Uveitis
Uveitis is an inflammation of the uveal tract of the eye, which includes the iris, ciliary body, and choroid. It is...
Uvulitis
Uvulitis is an inflammatory condition affecting the uvula, a small muscular structure that hangs from the back of the throat. It is a condition that...
Universal acquired melanosis
Universal acquired melanosis (UAM) is a skin condition characterized by hyperpigmentation that occurs in...
Unicentric Castleman disease (UCD)
Unicentric Castleman disease (UCD) is a rare disorder of the lymphatic system characterized by hyperplasia of the lymph...
Ureterocele
Ureterocele is an anomaly of the anatomical structure of the ureter, consisting of the formation of a sac-like protrusion, which...
Urethritis
Urethritis is an inflammation of the urethra, the tube that carries urine from the bladder and, in men, semen. It is a conditi...
Upper tract urothelial carcinoma (UTUC)
Upper tract urothelial carcinoma (UTUC) is a malignant neoplasm arising from the urothelial...
Ventricular fibrillation
Ventricular fibrillation (VF) is a serious and life-threatening condition characterized by chaotic, ineffective heartbeats...
Yaws
Yaws is a rare infectious disease caused by parasitic protozoa of the genus Leishmania, affecting the skin and mucous membranes ...
X-linked visceral heterotaxy 1
X-linked visceral heterotaxy (XLVH) is a rare genetic disorder that is a developmental disorder associated with...
X-linked hypophosphatemia
X-linked hypophosphatemia (XLH) is an inherited disorder characterized by abnormal...
X-linked cardiac valvular dysplasia
X-linked valvular dysplasia is a rare inherited disorder characterized by abnormal development of the heart valvular...
X-linked retinal dysplasia
X-linked retinal dysplasia (XLRD) is a rare inherited disorder characterized by abnormal development of the retina...
X-linked dominant scapuloperoneal myopathy
X-linked dominant scapuloperoneal myopathy (XLDPM) is a rare inherited disorder characterized by...
X-linked chondrodysplasia punctata 2
X-linked chondrodysplasia punctata 2 (HCH2) is a rare genetic disorder that belongs to the group of chondrodysplasias...
X-linked lymphoproliferative disorder
X-linked lymphoproliferative disorder (XLPD) is a rare genetic disorder characterized by abnormal reg...
X-linked infantile nystagmus
X-linked infantile nystagmus (XLN) is an inherited disorder characterized by characteristic eye movements that...
X-linked ichthyosis
X-linked ichthyosis is a genetic skin disease belonging to the group of ichthyoses, characterized by a violation of the keratinization of the epiderm...
X-linked retinitis pigmentosa (XLRP)
X-linked retinitis pigmentosa (XLRP) is an inherited disorder that belongs to a group of retinopathies characterized by progressive...
