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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 7,801-7,820 of 10,888 diseases
MONDO:0017047
MONDO:0015518
Infantile bilateral striatal necrosis is a condition characterized by symmetric spongy degeneration in deep brain structures such as the caudate nucle...
MONDO:0013802
Infantile cerebellar-retinal degeneration is a congenital condition that primarily affects the brain and eyes. The condition is caused by mutations in...
MONDO:0013351
MONDO:0008981
MONDO:0011178
Infantile convulsions and choreoathetosis is a neurological disorder that presents with seizures during the first year of life and abnormal involuntar...
MONDO:0016039
Infantile digital fibromatosis is a benign condition characterized by the development of nodular lesions on the fingers or toes, most often noticed in...
MONDO:0020071
Infantile epilepsy syndrome is an epilepsy condition that occurs between 28 days and one year of age, primarily impacting the developing brain. It is...
MONDO:0018226
MONDO:0017354
MONDO:0016223
MONDO:0014162
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency is a rare mitochondrial oxidative phosphorylation disorder that primarily affects the h...
MONDO:1010169
Infantile hypophosphatasia is a very rare and severe form of hypophosphatasia that primarily affects infants, manifesting as rickets without the typic...
MONDO:0033864
Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome, also known as Baker-Gordon syndrome, is a very rare neur...
MONDO:0016089
Infantile Krabbe disease, also known as classic or early-onset Krabbe disease, is a severe neurological disorder characterized by the degeneration of...
MONDO:0000023
Infantile liver failure is a very rare condition affecting the liver in early life, with cases estimated to occur in fewer than 1 in 1,000,000 people....
MONDO:0024568
Infantile liver failure syndrome 1 is a rare condition characterized by severe liver dysfunction in infancy that results from pathogenic variants in t...
MONDO:0014659
Infantile liver failure syndrome 2 is a condition characterized by liver failure in infancy caused by mutations in the NBAS gene. It primarily affects...
MONDO:0032844
Infantile liver failure syndrome 3 is a condition that primarily affects the liver and is also associated with distinct skeletal abnormalities. It is...
MONDO:0016588
Infantile mercury poisoning is a condition caused by exposure to mercury, which can be elemental, organic, or inorganic in form. It primarily affects...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.