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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 921-940 of 10,888 diseases
MONDO:0008780
Amyotrophic lateral sclerosis type 2, juvenile is an inherited motor neuron disorder caused by mutations in the ALS2 gene. It primarily affects childr...
MONDO:0011691
Amyotrophic lateral sclerosis type 3 (ALS3) is characterized by an autosomal dominant inheritance pattern, meaning that a single copy of the mutated g...
MONDO:0011223
Amyotrophic lateral sclerosis type 4 is a neurological condition primarily affecting the motor neurons, leading to progressive muscle weakness and deg...
MONDO:0011196
Amyotrophic lateral sclerosis type 5 is a motor neuron disease caused by mutations in the SPG11 gene. This condition primarily affects the neurons res...
MONDO:0011951
Amyotrophic lateral sclerosis type 6 is a form of a neurodegenerative disorder that primarily affects the motor neurons and leads to progressive muscl...
MONDO:0011952
Amyotrophic lateral sclerosis type 7 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0012077
Amyotrophic lateral sclerosis type 8 is a neurological condition that primarily affects the motor neurons responsible for controlling voluntary muscle...
MONDO:0012753
Amyotrophic lateral sclerosis type 9 (ALS9) is a form of amyotrophic lateral sclerosis caused by mutations in the ANG gene. This condition is inherite...
MONDO:0008782
Amyotrophic lateral sclerosis with polyglucosan bodies is an extremely rare condition. Because few cases have been documented, detailed clinical infor...
MONDO:0008076
Amyotrophic neuralgia is an inherited form of recurrent focal neuropathy that primarily affects the brachial plexus, leading to episodes of severe pai...
MONDO:0002000
Anaerobic meningitis is a condition characterized by inflammation of the meninges due to infection with anaerobic bacteria. It affects the central ner...
MONDO:0002735
Anal canal adenocarcinoma is a malignant tumor arising from the glandular epithelium of the anal canal mucosa that shares morphological characteristic...
MONDO:0007108
Anal canal carcinoma is a malignancy that arises from the epithelial cells of the anal canal. Recognized subtypes – including cloacogenic carcinoma, a...
MONDO:0004707
Anal canal carcinoma in situ is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0003504
Anal canal neuroendocrine neoplasm is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0004468
anal canal Paget disease is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0004132
Anal canal squamous cell carcinoma is a malignant cancer arising from the squamous cells lining the anal canal. This condition affects the lower gastr...
MONDO:0002940
Anal margin basal cell carcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0001470
Anal margin squamous cell carcinoma is a malignancy that arises from the perianal skin. Recognized subtypes are noted, with anal margin basal cell car...
MONDO:0006081
Anal melanoma is a malignant tumor that arises from the pigmented cells in the anal region. It typically presents with symptoms affecting the anorecta...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.