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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 7,221-7,240 of 10,888 diseases
MONDO:0017658
Hyperekplexia is a neurologic disorder characterized by pronounced startle responses to unexpected tactile or acoustic stimuli and increased muscle to...
MONDO:0007868
Hyperekplexia 1 is an inherited neurological condition primarily characterized by an exaggerated startle response and muscle stiffness. It is caused b...
MONDO:0013828
Hyperekplexia 2 is a hereditary neurological condition caused by mutations in the GLRB gene. It is characterized by an exaggerated startle response an...
MONDO:0013827
Hyperekplexia 3 is a hereditary neurological condition characterized primarily by an exaggerated startle response, which is always present. It is caus...
MONDO:0044330
Hyperekplexia 4 is a severe neurologic disorder that becomes apparent at birth, with affected infants displaying extreme rigidity and a lack of sponta...
MONDO:0100059
Hypereosinophilia of undetermined significance is a condition characterized by a prolonged elevation of eosinophil counts in the blood without an iden...
MONDO:0015691
Hypereosinophilic syndrome (HES) is a group of disorders characterized by persistently high levels of eosinophils in the blood and tissues, which can...
MONDO:0006792
Hyperglobulinemic purpura is a condition characterized by a purplish or brownish red discoloration of the skin, most often observed on the legs. It is...
MONDO:0800331
MONDO:0009417
MONDO:0004743
Hyperhomocysteinemia is a serious metabolic condition characterized by elevated levels of homocysteine in the blood, which increases the risk of blood...
MONDO:0007818
Hyper-IgE recurrent infection syndrome 1 is a condition characterized by immune dysregulation and recurrent infections, primarily affecting the skin a...
MONDO:0032654
Hyper-IgE recurrent infection syndrome 3 is a rare immunologic disorder characterized by high levels of immunoglobulin E, recurring skin infections, a...
MONDO:0800131
MONDO:0032796
Hyper-IgE recurrent infection syndrome 4, autosomal recessive is a multisystem condition that affects immune regulation, skeletal development, craniof...
MONDO:0030069
Hyper-IgE recurrent infection syndrome 5, autosomal recessive is an immune dysregulation condition characterized by elevated interleukin 6 and IgE lev...
MONDO:0018037
Hyper-IgE syndrome is a condition characterized by elevated serum IgE levels, chronic skin inflammation, and recurrent respiratory infections. It is a...
MONDO:0957807
MONDO:0003947
Hyper-IgM syndrome is a primary immunodeficiency disorder that impairs the immune system’s ability to produce a diverse range of antibodies. This diso...
MONDO:0010626
Hyper-IgM syndrome type 1 is an immunodeficiency disorder characterized by a failure in immunoglobulin class switching, which leads to decreased level...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.