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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 6,921-6,940 of 10,888 diseases
MONDO:0016249
MONDO:0700223
Hereditary skeletal muscle disorder is an inherited condition affecting the muscle tissue. It results from genomic modifications in several genes know...
MONDO:0019064
Hereditary spastic paraplegia (HSP) is a group of neurodegenerative disorders that are both genetically and clinically diverse. People with this condi...
MONDO:0011408
Hereditary spastic paraplegia 10, also known as SPG10, is a type of genetic disorder that primarily affects the motor system, leading to progressive s...
MONDO:0011445
Hereditary spastic paraplegia 11 is an inherited disorder that primarily affects the motor system and aspects of cognitive development. It is caused b...
MONDO:0011489
Hereditary spastic paraplegia 12 is a neurological condition characterized by slowly progressive spasticity predominantly affecting the lower limbs. I...
MONDO:0011532
MONDO:0011522
MONDO:0010044
Hereditary spastic paraplegia 15 is a complex neurological condition marked by slowly progressive stiffness and weakness in the lower limbs. It is cau...
MONDO:0010287
Hereditary spastic paraplegia 16 is a neurological condition marked by progressive muscle stiffness and weakness, predominantly affecting limb movemen...
MONDO:0010043
Hereditary spastic paraplegia 17 is an inherited neurological disorder that primarily affects the motor system, leading to stiffness and weakness pred...
MONDO:0012639
Hereditary spastic paraplegia 18 is a rare and complex neurodevelopmental condition characterized by progressive spasticity in the lower limbs, signif...
MONDO:0011785
Hereditary spastic paraplegia 19 is a neurological condition characterized by a slowly progressive spastic paraplegia that primarily affects the lower...
MONDO:0010733
Hereditary spastic paraplegia 2 is an X-linked leukodystrophy that primarily affects the central nervous system, leading to spastic gait and signs of...
MONDO:0010046
Hereditary spastic paraplegia 23 is a complex neurological condition that presents in childhood with progressive spasticity of the legs and distinctiv...
MONDO:0011862
MONDO:0011992
Hereditary spastic paraplegia 25, also known as SPG25, is a complex condition affecting the spinal cord that typically presents in adulthood with spas...
MONDO:0012213
Hereditary spastic paraplegia 26 is a rare neurogenetic disorder that primarily affects motor function and aspects of cognitive development. It is cau...
MONDO:0012181
MONDO:0012256
Hereditary spastic paraplegia 28 is a pure form of hereditary spastic paraplegia that primarily affects the musculature, nervous system, and skeletal...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.