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 8,761-8,780 of 10,888 diseases
MONDO:0015524
MONDO:0023419
Hyperprolinemia is a metabolic condition characterized by an elevated level of the amino acid proline in the blood. It results from a disruption in th...
MONDO:0009400
MONDO:0009401
MONDO:0017853
Hypersensitivity pneumonitis is a lung condition characterized by an inflammatory reaction in the lungs due to repeated inhalation of environmental an...
MONDO:0007776
Hypersensitivity pneumonitis, familial is an inherited lung condition in which the immune system reacts abnormally to airborne environmental antigens....
MONDO:0006794
Hypersensitivity vasculitis is a condition characterized by inflammation of the small blood vessels, most in the skin and, in some cases, internal org...
MONDO:0006795
Hypersplenism is a condition characterized by an overactive spleen that leads to the excessive destruction of blood cells. This abnormal spleen functi...
MONDO:0009404
MONDO:0013614
MONDO:0019280
Hypertrichosis is a condition defined by excessive hair growth anywhere on the body. Although its precise prevalence is not well established, the cond...
MONDO:0007693
Hypertrichosis cubiti-short stature syndrome is a condition primarily characterized by unusually dense hair growth localized to the extensor surfaces...
MONDO:0016381
Hypertrichosis lanuginosa congenita is a rare congenital skin condition marked by the presence of unusually long, soft lanugo-type hair covering almos...
MONDO:0001334
Hypertrichosis of the eyelid is a condition characterized by an unusual overgrowth of hair on the eyelid. It is a localized form of hypertrichosis tha...
MONDO:0019940
MONDO:0009406
MONDO:0007788
MONDO:0859149
MONDO:0005045
Hypertrophic cardiomyopathy is a condition in which the heart muscle, or myocardium, becomes unusually thick without an obvious cause. This thickening...
MONDO:0008647
Hypertrophic cardiomyopathy 1 is a condition of the heart muscle that results from a mutation in the MYH7 gene, one of the genes linked to abnormal ca...
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