Trusted information across 10,888 rare diseases — plain language, always cited, free for everyone.
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Data syncs range from 3x daily (news) to weekly (trials, FDA). Reports regenerate when data changes.
Showing 8,601-8,620 of 10,888 diseases
MONDO:0018328
Homozygous familial hypercholesterolemia (HoFH) is a rare genetic condition characterized by extremely high levels of low-density lipoprotein (LDL) ch...
MONDO:0020363
MONDO:0011810
MONDO:0013229
MONDO:0020535
MONDO:0005459
Human African trypanosomiasis is a parasitic infection caused by protozoa of the Trypanosoma brucei species and is transmitted by the bite of tsetse f...
MONDO:0011099
MONDO:0005801
Human T-lymphotropic virus 1 infectious disease is a viral infection that affects the immune system, particularly the CD4 lymphocytes. The disease is...
MONDO:0700096
Human disease is a broad term covering a range of conditions for which detailed clinical and biological features remain largely unspecified. Because d...
MONDO:0005118
Human granulocytic anaplasmosis is a tick‐borne infectious disease caused by the bacterium Anaplasma phagocytophilum, which is transmitted to humans b...
MONDO:0015157
Human herpesvirus 8-related tumor is a condition characterized by abnormal growths that arise in association with infection by human herpesvirus 8. Th...
MONDO:0018583
Human infection by orthopoxvirus is a viral condition caused by an orthopoxvirus and is classified as an infectious disorder. Although detailed inform...
MONDO:0000225
Human monocytic ehrlichiosis is an infection caused by the bacterium Ehrlichia chaffeensis, an obligate intracellular pathogen that targets monocytes...
MONDO:0020656
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...
MONDO:0020657
Human papillomavirus-related squamous cell carcinoma is a malignant tumor that arises from squamous cells and is linked to human papillomavirus infect...
MONDO:0018926
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...
MONDO:0017440
Humeral agenesis/hypoplasia is a congenital limb reduction defect characterized by the absence or underdevelopment of the humerus, which can affect on...
MONDO:0017483
MONDO:0017482
MONDO:0017551
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