Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 8 more sources. Updated daily.
Showing 10,081-10,100 of 10,888 diseases
MONDO:0800027
Leukoencephalopathy, diffuse hereditary, with spheroids 1 is a very rare inherited neurological condition that damages the white matter of the brain a...
MONDO:0030634
MONDO:0958226
MONDO:0014387
Leukoencephalopathy, progressive, with ovarian failure is a disorder that primarily affects the nervous system and ovarian function. It is caused by p...
MONDO:0016545
MONDO:0013971
Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome is a rare genetic neurological disorder that affects the white matter of th...
MONDO:0016557
MONDO:0016213
MONDO:0003785
Leukopenia is a laboratory finding that indicates a decreased number of white blood cells in the peripheral blood, which are essential for fighting in...
MONDO:0006831
MONDO:0019862
MONDO:0018856
Lichen amyloidosis is a rare chronic form of cutaneous amyloidosis, a skin condition characterized by the deposition of amyloid in the dermis, which r...
MONDO:0018432
Lichen myxedematosus is a skin disorder marked by changes in the skin's texture and the appearance of papules, often described as mucin deposits. Alth...
MONDO:0018879
MONDO:0016775
MONDO:0016774
MONDO:0045044
Ligament disorder is a condition that affects the connective tissues responsible for stabilizing joints. It involves abnormalities of the ligament, wh...
MONDO:0019729
Light and heavy chain deposition disease, also known as LHCDD, is a condition characterized by the abnormal deposition of protein components in tissue...
MONDO:0019730
Light chain deposition disease is a rare condition in which small protein fragments called light chains accumulate in the kidneys and can also affect...
MONDO:0016528
Structured data for researchers, pharma, and clinical teams
Structured disease data via API. AI reports on demand. Phenotypes, genes, orphan drug designations, screening status, and PAG mapping.