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 7,681-7,700 of 10,888 diseases
MONDO:0016068
Fibrochondrogenesis is a severe skeletal dysplasia and chondrodysplasia that affects newborns, with a striking presentation at birth. It is linked to...
MONDO:0009226
Fibrochondrogenesis 1 is a severe genetic disorder affecting skeletal development, caused by mutations in the COL11A1 gene. It involves abnormal forma...
MONDO:0013795
MONDO:0007606
Fibrodysplasia ossificans progressiva (FOP) is a severely disabling connective-tissue disorder in which muscles, tendons, and other soft tissues gradu...
MONDO:0035312
MONDO:0006210
Fibrolamellar hepatocellular carcinoma is a distinctive form of liver cancer that arises in non-cirrhotic livers and is most often seen in younger ind...
MONDO:0007609
MONDO:0011563
MONDO:0012378
MONDO:0012598
MONDO:0033493
MONDO:0975841
MONDO:0007671
MONDO:0970961
MONDO:0005164
Fibrosarcoma is a malignant tumor arising from fibrous connective tissue that can affect both soft tissues and bone. This condition is characterized a...
MONDO:0004301
MONDO:0009230
MONDO:0011181
Fibrosis of extraocular muscles, congenital, 2 is a condition in which abnormal fibrotic changes of the eye muscles are present from birth, affecting...
MONDO:0010912
Fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement is a condition present at birth that primarily affects the mu...
MONDO:0800209
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