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Rare Disease Intelligence — 10,888 conditions monitored | Kisho | Kisho

Open data · 12 authoritative sources

Find your disease.
What’s known, in plain language.

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.

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Commonly searched:Cystic Fibrosis Duchenne Huntington's ALS Sickle Cell

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12

authoritative sources — clinical, regulatory, scientific

10,888

rare conditions, continuously monitored

Daily

updates from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet…

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Showing 2,861-2,880 of 10,888 diseases

cervical villoglandular adenocarcinoma

MONDO:0006141

Cervical villoglandular adenocarcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limite...

cervicofacial actinomycosis

MONDO:0005699

Cervicofacial actinomycosis is an acquired infectious condition that primarily affects the tissues of the head and neck, particularly the lymph nodes...

cervicofacial fibrochondroma

MONDO:0015383

Cervicofacial fibrochondroma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

cervicothoracic spina bifida aperta

MONDO:0017067

cervicothoracic spina bifida aperta is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

cervicothoracic spina bifida cystica

MONDO:0017074

cervicothoracic spina bifida cystica is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

cesium poisoning

MONDO:0800384

Cesium poisoning is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

CFAP418-related ciliopathy

MONDO:0700374

CFAP418-related ciliopathy is a condition caused by changes in the CFAP418 gene. This condition is linked with disorders such as Bardet-Biedl syndrome...

CFAP46-related primary ciliary dyskinesia

MONDO:1010146

CFAP46-related primary ciliary dyskinesia is a rare form of primary ciliary dyskinesia that is caused by a mutation in the CFAP46 gene. This means tha...

CFTR-related metabolic syndrome

MONDO:0100627

CFTR-related metabolic syndrome is a metabolic condition identified in some infants who present with hypertrypsinogenemia on newborn screening. It is...

Chagas cardiomyopathy

MONDO:0005491

Chagas cardiomyopathy is a disease of the heart muscle that develops after a person is infected with the parasite Trypanosoma cruzi. Initially, some c...

Chagas disease

MONDO:0001444

Chagas disease is a parasitic infection caused by Trypanosoma cruzi that is transmitted through insect bites. The condition typically presents with an...

chancroid

MONDO:0001797

Chancroid is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It is a bacterial infectio...

Chandler syndrome

MONDO:0020369

Chandler syndrome is a form of iridocorneal endothelial (ICE) syndrome. It is the most common variant of ICE syndrome and is mainly noted for its impa...

CHAND syndrome

MONDO:0008959

CHAND syndrome, also known as CHANDS or curly hair-ankyloblepharon-nail dysplasia syndrome, is a rare condition. The condition is identified by its un...

channelopathy-associated congenital insensitivity to pain, autosomal recessive

MONDO:0009459

Channelopathy-associated congenital insensitivity to pain, autosomal recessive is a rare condition that affects the nervous system’s ability to transm...

chaotic conus spinal cord lipoma

MONDO:0968986

chaotic conus spinal cord lipoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It...

Chapare hemorrhagic fever

MONDO:0017878

Chapare hemorrhagic fever is an acute viral disease caused by the Chapare virus, a new arenavirus. It was first identified during a small outbreak in...

Charcot-Marie-Tooth disease

MONDO:0015626

Charcot-Marie-Tooth disease is an inherited disorder that affects the peripheral nerves responsible for communication between the brain and the limbs....

MFN2BAG3SLC12A6+7

Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;

MONDO:0014906

Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b is a genetic condition that affects the nerves. It is caused by changes in the MFN...

Charcot-Marie-Tooth disease, axonal, IIa 2II

MONDO:0031068

Charcot-Marie-Tooth disease, axonal, IIa 2II (also known as CMT2II) is a rare inherited disorder that affects the peripheral nerves, which are respons...

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