Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 8 more sources. Updated daily.
Showing 10,061-10,080 of 10,888 diseases
MONDO:0030263
Leukodystrophy, hypomyelinating, 21 is a neurological condition characterized by abnormalities in the brain’s white matter. It is caused by pathogenic...
MONDO:0025701
MONDO:0030514
MONDO:0859242
MONDO:0859378
MONDO:0859518
MONDO:0958018
Leukodystrophy, hypomyelinating, 27 is a neurological disorder characterized by abnormal white matter development and predominant central nervous syst...
MONDO:0975833
MONDO:0011897
MONDO:0015348
MONDO:0012622
Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome (LBSL) is a very rare inherited leukodystrophy that primarily af...
MONDO:0013803
MONDO:0014292
MONDO:0800448
Leukoencephalopathy with vanishing white matter (VWM) is a hereditary disorder that damages the brain’s white matter, the tissue responsible for rapid...
MONDO:0020507
Leukoencephalopathy with vanishing white matter 1 is a disorder affecting the brain's white matter, leading to progressive neurological impairment. It...
MONDO:0957870
MONDO:0957871
MONDO:0957872
MONDO:0957873
Leukoencephalopathy with vanishing white matter 5 is a neurological condition primarily affecting the brain's white matter, resulting in progressive n...
MONDO:0032716
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.