Kisho

Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy

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.

Search by:Disease•Gene•Symptom•Treatment•PAG•OMIM/Orphanet ID

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

Always free
Plain language
Sourced

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…

Browse by category:

Showing 881-900 of 10,888 diseases

amniotic band syndrome

MONDO:0015167

Amniotic band syndrome is a group of sporadic congenital anomalies that occur in association with fibrous amniotic bands, affecting the limbs, craniof...

amniotic fluid embolism

MONDO:0850046

Information about the overall nature of amniotic fluid embolism is currently limited for this condition. At times, the condition is noted in trusted r...

amoebiasis due to Entamoeba histolytica

MONDO:0019028

Amoebiasis due to Entamoeba histolytica is an infection caused by a parasitic protozoa that primarily affects the gastrointestinal system. The disease...

amoebiasis due to free-living amoebae

MONDO:0019036

Amoebiasis due to free-living amoebae is an infection primarily affecting the central nervous system, with the potential to cause devastating conditio...

ampulla of vater adenocarcinoma

MONDO:0002670

Ampulla of vater adenocarcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

ampulla of vater adenosquamous carcinoma

MONDO:0003553

Ampulla of vater adenosquamous carcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limi...

ampulla of vater cancer

MONDO:0000919

Ampulla of vater cancer is a malignant neoplasm involving the ampulla of Vater, a critical anatomical area where the bile and pancreatic ducts converg...

ampulla of vater clear cell adenocarcinoma

MONDO:0003388

Ampulla of vater clear cell adenocarcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is li...

ampulla of vater mucinous adenocarcinoma

MONDO:0002736

Ampulla of vater mucinous adenocarcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limi...

ampulla of vater small cell neuroendocrine carcinoma

MONDO:0004117

Ampulla of vater small cell neuroendocrine carcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical informa...

ampulla of vater squamous cell carcinoma

MONDO:0003490

Ampulla of vater squamous cell carcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limi...

ampullary signet ring cell adenocarcinoma

MONDO:0002669

Ampullary signet ring cell adenocarcinoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is lim...

amyloidosis

MONDO:0019065

Amyloidosis is a disorder characterized by the abnormal accumulation of amyloid protein in various tissues, which can be either localized or diffuse....

amyloidosis bronchopulmonary

MONDO:0022444

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

amyloidosis cutis dyschromia

MONDO:0017906

Amyloidosis cutis dyschromia is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

amyloidosis, hereditary systemic 1

MONDO:0971004

Amyloidosis, hereditary systemic 1 is a multisystem condition characterized primarily by the abnormal deposition of amyloid proteins, with increased c...

amyloidosis, hereditary systemic 3

MONDO:0971008

Amyloidosis, hereditary systemic 3 is a complex, multi-organ condition characterized by the abnormal deposition of amyloid proteins throughout the bod...

amyloidosis, hereditary systemic 5

MONDO:0971009

Hereditary systemic amyloidosis type 5 is a multisystem condition characterized by the abnormal deposition of amyloid proteins affecting several organ...

amyloidosis, hereditary systemic 6

MONDO:0971010

Hereditary systemic amyloidosis 6 is a multi‐system condition characterized by the abnormal deposition of amyloid proteins affecting several organ sys...

amyloidosis, primary localized cutaneous, 1

MONDO:0024522

Amyloidosis, primary localized cutaneous, 1 is a skin condition characterized by abnormal protein deposits in the skin. It is caused by a mutation in...

Previous45 / 545Next

Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.