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 2,741-2,760 of 10,888 diseases

central nervous system vasculitis

MONDO:0003346

Central nervous system vasculitis is a condition in which the blood vessels of the brain and spinal cord become inflamed. This inflammation can disrup...

central neurocytoma

MONDO:0019134

Central neurocytoma is a rare brain tumor predominantly affecting young adults, with over 100 cases documented globally. It is typically located in th...

central polydactyly of fingers

MONDO:0017456

Central polydactyly of fingers is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

central polydactyly of fingers, bilateral

MONDO:0017536

Central polydactyly of fingers, bilateral is an extremely rare condition. Because few cases have been documented, detailed clinical information is lim...

central polydactyly of fingers, unilateral

MONDO:0017535

Central polydactyly of fingers, unilateral is an extremely rare condition. Because few cases have been documented, detailed clinical information is li...

central precocious puberty

MONDO:0019165

Central precocious puberty is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

central precocious puberty 1

MONDO:0008302

Central precocious puberty 1 is a form of early-onset puberty that occurs when pubertal development begins earlier than expected. This condition is ca...

central precocious puberty in male

MONDO:0958270

Central precocious puberty in male is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

central retinal vein occlusion with macular edema

MONDO:0041093

Central retinal vein occlusion with macular edema is an extremely rare condition. Because few cases have been documented, detailed clinical informatio...

central serous chorioretinopathy

MONDO:0018616

Central serous chorioretinopathy is an eye condition characterized by a buildup of fluid under the retina, which can lead to blurred or distorted cent...

centrifugal lipodystrophy

MONDO:0019552

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

centripetalis recessive dystrophic epidermolysis bullosa

MONDO:0019521

Centripetalis recessive dystrophic epidermolysis bullosa (RDEB-Ce) is an extremely rare subtype of dystrophic epidermolysis bullosa characterized by b...

centronuclear myopathy

MONDO:0018947

Centronuclear myopathy (CNM) is a rare inherited neuromuscular disorder characterized by muscle weakness and centrally placed nuclei in muscle fibers,...

MTM1MAP3K20CCDC78+1

CEP164-related ciliopathy

MONDO:0700344

CEP164-related ciliopathy is a rare condition caused by changes in the CEP164 gene. It is a type of ciliopathy, which means it involves problems with...

CEP290-related ciliopathy

MONDO:0100451

CEP290-related ciliopathy is a condition that affects the tiny structures in cells called cilia. Cilia are important for many body systems, and when t...

cephalocele

MONDO:0017078

Cephalocele is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It is characterized by a...

cercarial dermatitis

MONDO:0001260

Cercarial dermatitis is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It is character...

cerebellar astrocytoma

MONDO:0003165

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

cerebellar ataxia

MONDO:0000437

Cerebellar ataxia is a neurological syndrome characterized by clumsy and uncoordinated movements of the limbs, trunk, and muscles involved in speech a...

cerebellar ataxia and hypergonadotropic hypogonadism

MONDO:0011580

Cerebellar ataxia and hypergonadotropic hypogonadism is an extremely rare condition. Because few cases have been documented, detailed clinical informa...

Previous138 / 545Next

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