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 9,301-9,320 of 10,888 diseases
MONDO:0016534
MONDO:0011465
MONDO:0016595
Inhalational anthrax is a rare and severe infection caused by inhaling spores of the bacterium Bacillus anthracis, often associated with exposure to i...
MONDO:0016777
Inhalational botulism is a man-made form of botulism that affects the neuromuscular junction, leading to a descending flaccid paralysis. It results fr...
MONDO:0007403
Inherited Creutzfeldt-Jakob disease is a very rare genetic prion disorder that affects the brain, leading to rapidly progressive dementia along with b...
MONDO:0100238
Inherited Fanconi renotubular syndrome is a condition that affects the kidney’s ability to reabsorb essential substances, leading to renal tubular dys...
MONDO:0017893
Inherited acute myeloid leukemia is a form of acute myeloid leukemia that arises due to an inherited change in the genome. This condition affects the...
MONDO:0001713
Inherited aplastic anemia is an inborn condition characterized by a deficiency of red blood cell precursors that can sometimes include low levels of w...
MONDO:0000009
Inherited bleeding disorder, platelet-type is a condition characterized by abnormal platelet function leading to an increased tendency for bleeding. A...
MONDO:0021181
Inherited blood coagulation disorder is a condition that affects the blood’s ability to clot normally, which can lead to complications from either exc...
MONDO:0100237
Inherited cutis laxa is an inherited condition characterized by abnormalities in the skin’s elasticity and the structure of connective tissue. Althoug...
MONDO:1060161
MONDO:0044807
Inherited dystonia is a type of dystonic disorder that results from an inherited alteration in the individual’s genome. It is characterized by abnorma...
MONDO:0019276
Inherited epidermolysis bullosa is a group of disorders marked by recurrent blister formation due to inherent structural fragility of the skin and, in...
MONDO:0037858
Inherited fatty acid metabolism disorder is a group of genetic conditions characterized by the body’s inability to properly oxidize fatty acids for en...
MONDO:0005363
Inherited focal segmental glomerulosclerosis (FSGS) is a kidney disorder linked to genetic variants in several genes, including TRPC6, ANLN, MYO1E, PA...
MONDO:0040566
Inherited glutathione metabolism disease is an inherited metabolic condition characterized by a disruption in the glutathione metabolic process, which...
MONDO:0017909
Inherited glutathione synthetase deficiency is a metabolic condition that primarily affects the production of glutathione, a critical molecule for cel...
MONDO:0850064
MONDO:0019050
Inherited hemoglobinopathy is an inherited disorder characterized by structural alterations in one of the globin chains of the hemoglobin molecule. Th...
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