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Plain-language summaries of 10,888 rare conditions, drawn from MONDO, GeneReviews, ClinVar, FDA, NIH, ClinicalTrials.gov, PubMed, and 5 other public sources. Free, sourced, never gated.
Kisho provides public health information only — not medical advice. Always consult your healthcare provider.
12
authoritative sources — clinical, regulatory, scientific
10,888
rare conditions, continuously monitored
Daily
updates from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet…
Showing 8,841-8,860 of 10,888 diseases
MONDO:0033657
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
Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism is a disorder affecting the central nervous syste...
MONDO:0032716
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:0016545
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:0013971
Leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome is a rare genetic neurological disorder that affects the white matter of th...
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
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.