Trusted information across 10,888 rare diseases — plain language, always cited, free for everyone.
Can't find your disease? Try searching by gene, symptom, or OMIM ID.
Every report passes a 3-tier quality pipeline with gene validation, fact-checking, and safety checks.
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and more. Every claim is cited.
Data syncs range from 3x daily (news) to weekly (trials, FDA). Reports regenerate when data changes.
Showing 8,861-8,880 of 10,888 diseases
MONDO:0009150
MONDO:0009416
Hypoinsulinemic hypoglycemia and body hemihypertrophy is a very rare condition that affects metabolic regulation and body growth, characterized by low...
MONDO:0008223
Hypokalemic periodic paralysis is a condition that presents with episodic muscle paralysis lasting for a few hours up to 24-48 hours, typically trigge...
MONDO:0042979
MONDO:0013234
Hypokalemic periodic paralysis, type 2 is a neuromuscular condition characterized by episodes of muscle weakness associated with low blood potassium l...
MONDO:0001822
Hypolipoproteinemia is a condition characterized by abnormally low levels of lipoproteins in the blood, affecting the transport of cholesterol and oth...
MONDO:0859328
Hypomagnesemia 7, renal, with or without dilated cardiomyopathy is an inherited condition that primarily affects kidney function and the heart. It is...
MONDO:0014631
MONDO:0020787
MONDO:0020788
MONDO:0009425
MONDO:0007093
MONDO:0014632
MONDO:0014666
MONDO:0014732
MONDO:0014813
MONDO:0012125
MONDO:0009843
MONDO:0012824
MONDO:0012514
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