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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 10,301-10,320 of 10,888 diseases
MONDO:0018939
Muscle-eye-brain disease is a congenital muscular dystrophy characterized by early onset muscle weakness and distinctive malformations of the brain an...
MONDO:0018280
MONDO:0003939
Muscle tissue disorder is a condition primarily affecting the muscle tissue, with the underlying biology linked to the MSTN gene. The MSTN gene plays...
MONDO:0004323
Muscular atrophy is a condition characterized by the loss of muscle tissue due to inactivity or disease. It primarily affects the muscles, leading to...
MONDO:0008023
Muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome is an autosomal dominant disorder characterized by a combination of muscular a...
MONDO:0019119
Muscular channelopathy is a condition that affects the muscle tissue through abnormalities in ion channel function. It has been linked to changes in t...
MONDO:0020121
Muscular dystrophy refers to a group of more than 30 genetic disorders that are primarily characterized by progressive weakening and degeneration of t...
MONDO:0008028
Muscular dystrophy, Barnes type is a condition primarily affecting muscle function, where muscle weakness and loss of mobility can be prominent featur...
MONDO:0010675
Muscular dystrophy, cardiac type is a disorder that primarily affects the muscles of the heart and may also involve skeletal muscles. Although a clear...
MONDO:0009682
Muscular dystrophy, congenital, with rapid progression is a condition affecting muscle development and function from early in life. It is classified a...
MONDO:0018276
Muscular dystrophy-dystroglycanopathy is a congenital disorder that primarily affects muscle development and function. This condition is linked to alt...
MONDO:0009364
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1 is a severe neuromuscular disorder that affects multiple orga...
MONDO:0014022
MONDO:0014071
MONDO:0014101
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12 is a condition that affects both muscle function and brain...
MONDO:0014120
MONDO:0014140
MONDO:0013154
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2 is a severe congenital disorder that primarily affects muscle...
MONDO:0009667
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3 is a severe neuromuscular disorder that affects both muscle f...
MONDO:0009678
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 is a congenital progressive condition that primarily affect...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.