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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 2,821-2,840 of 10,888 diseases
MONDO:0024564
Cerebroretinal microangiopathy with calcifications and cysts 1 is a multisystem condition that primarily affects the brain and the retina, and is asso...
MONDO:0015026
Cerebroretinal microangiopathy with calcifications and cysts 2 is a multisystem disorder that affects the brain, eyes, blood, liver, and gastrointesti...
MONDO:0957264
Cerebroretinal microangiopathy with calcifications and cysts 3 is a multisystem condition that affects the brain, eyes, and other organ systems. It is...
MONDO:0008948
Cerebrotendinous xanthomatosis (CTX) is a disorder of bile acid synthesis that affects multiple systems including the liver, eyes, tendons, and brain....
MONDO:0800401
CERKL-related retinopathy is an inherited eye condition that impacts the retina, the light-sensitive layer at the back of the eye. It is caused by cha...
MONDO:0012650
Cernunnos-XLF deficiency is a rare form of combined immunodeficiency. This condition is characterized by a smaller than usual head (microcephaly), slo...
MONDO:0008083
Ceroid lipofuscinosis, neuronal, 4 (Kufs type) is a neurodegenerative condition characterized by the accumulation of intracellular lipopigments and is...
MONDO:0011144
Ceroid lipofuscinosis, neuronal, 6A (CLN6) is a rare neurodegenerative disorder caused by mutations in the CLN6 gene, inherited in an autosomal recess...
MONDO:0008768
Ceroid lipofuscinosis, neuronal, 6B (Kufs type) is a neurodegenerative disorder that primarily affects the central nervous system, leading to progress...
MONDO:0020374
Cerulean cataract is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It is characterize...
MONDO:0005153
Cervical adenocarcinoma is a form of cancer that arises from the glandular cells lining the cervix. It comprises approximately 15% of invasive cervica...
MONDO:0006132
Cervical adenoid basal carcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0006133
Cervical adenoid cystic carcinoma is a rare type of cancer that originates from the cervix. It is characterized by distinctive microscopic features, i...
MONDO:0002876
Cervical adenosarcoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0006134
Cervical adenosquamous carcinoma is an uncommon malignancy of the cervix that shows features of both glandular and squamous cell carcinomas. Recognize...
MONDO:0004542
Cervical adenosquamous carcinoma, glassy cell variant is an extremely rare condition. Because few cases have been documented, detailed clinical inform...
MONDO:0003003
Cervical alveolar soft part sarcoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0004088
Cervical basaloid carcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0002877
Cervical carcinosarcoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0006135
Cervical clear cell adenocarcinoma is a rare morphologic variant of cervical adenocarcinoma that involves the clear and hobnail cell types within the...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.