Hoyeraal-Hreidarsson syndrome is a very rare disorder that is usually passed down on the X chromosome. It is considered a severe form of dyskeratosis...

HSD10 disease, atypical type is a rare condition that is also known by several names, including X-linked intellectual disability-choreoathetosis-abnor...

HSD10 disease, infantile type is a rare neurometabolic disorder that typically shows normal development until about 6 to 18 months of age. After this...

HSD10 disease, neonatal type is the most severe form of HSD10 disease, a rare neurometabolic disorder. It typically appears in the neonatal period, a...

HSD10 mitochondrial disease is a rare, life-threatening neurometabolic condition that primarily affects the nervous system. Recognized subtypes, inclu...

H syndrome is an inherited condition that affects multiple parts of the body. It is characterized by particular skin changes along with effects on int...

HTRA1-related autosomal dominant cerebral small vessel disease, also known as HTRA1-related autosomal dominant cerebral angiopathy, is a rare conditio...

Hughes-Stovin syndrome is a life-threatening vascular disorder characterized by the presence of multiple pulmonary artery aneurysms and peripheral ven...

Human African trypanosomiasis is a parasitic infection caused by protozoa of the Trypanosoma brucei species and is transmitted by the bite of tsetse f...

Human disease is a broad term covering a range of conditions for which detailed clinical and biological features remain largely unspecified. Because d...

Human granulocytic anaplasmosis is a tick‐borne infectious disease caused by the bacterium Anaplasma phagocytophilum, which is transmitted to humans b...

Human herpesvirus 8-related tumor is a condition characterized by abnormal growths that arise in association with infection by human herpesvirus 8. Th...

Human infection by orthopoxvirus is a viral condition caused by an orthopoxvirus and is classified as an infectious disorder. Although detailed inform...

Human monocytic ehrlichiosis is an infection caused by the bacterium Ehrlichia chaffeensis, an obligate intracellular pathogen that targets monocytes...

Human papillomavirus-related penile squamous cell carcinoma is a type of cancer that arises on the penis as a result of an infection with human papill...

Human papillomavirus-related squamous cell carcinoma is a malignant tumor that arises from squamous cells and is linked to human papillomavirus infect...

Human prion disease is a rare neurological condition that belongs to a group of disorders characterized by spongiform changes in the brain. It is caus...

Human T-lymphotropic virus 1 infectious disease is a viral infection that affects the immune system, particularly the CD4 lymphocytes. The disease is...

Humeral agenesis/hypoplasia is a congenital limb reduction defect characterized by the absence or underdevelopment of the humerus, which can affect on...