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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 5,041-5,060 of 10,888 diseases
MONDO:0001342
Dysgammaglobulinemia is an immunologic deficiency state characterized by the selective deficiency of one or more classes of immunoglobulins. Because t...
MONDO:0003002
Dysgerminoma is a malignant germ cell tumor that primarily arises in the ovaries, although it can also develop in other sites such as the central nerv...
MONDO:0003481
Dysgerminoma of the ovary is a malignant germ cell tumor that arises in the female reproductive system. It is histologically similar to seminoma, feat...
MONDO:0015780
Dyskeratosis congenita (DC) is a rare ectodermal dysplasia characterized by a classic triad of nail dysplasia, skin pigmentary changes, and oral leuko...
MONDO:0800467
Dyskeratosis congenita and related telomere biology disorder is a condition that primarily affects the skin, nails, and bone marrow, reflecting its br...
MONDO:0007485
Dyskeratosis congenita, autosomal dominant 1 is an inherited condition primarily caused by a mutation in the TERC gene. It is characterized by abnorma...
MONDO:0013521
Dyskeratosis congenita, autosomal dominant 2 is a multisystem disorder linked to abnormalities in telomere maintenance caused by changes in the TERT g...
MONDO:0013522
Dyskeratosis congenita, autosomal dominant 3 is a multi-system condition caused by alterations in the TINF2 gene, which plays a critical role in telom...
MONDO:0800366
dyskeratosis congenita, autosomal dominant 4 (also known as DKCA4) is a condition that affects multiple organ systems, although specific details about...
MONDO:0014690
Dyskeratosis congenita, autosomal dominant 6 is a genetic condition affecting multiple systems, with its biological basis linked to changes in the ACD...
MONDO:0009136
Dyskeratosis congenita, autosomal recessive 1 is an inherited condition marked by distinctive skin changes and blood abnormalities. Individuals typica...
MONDO:0013519
Dyskeratosis congenita, autosomal recessive 2 is a multisystem condition that primarily impacts the skin, nail structures, bone marrow, and other orga...
MONDO:0013520
Dyskeratosis congenita, autosomal recessive 3 is an inherited condition primarily affecting the skin, nails, oral mucosa, and bone marrow, with a pred...
MONDO:0014076
Dyskeratosis congenita, autosomal recessive 5 is a multi-system condition that primarily affects neurodevelopment and other organ systems. It is linke...
MONDO:0014600
Dyskeratosis congenita, autosomal recessive 6 is a rare inherited disorder caused by mutations in the PARN gene. This condition affects multiple organ...
MONDO:0800370
Dyskeratosis congenita, autosomal recessive 7 is a condition that has been recognized based on clinical observations, although many details about its...
MONDO:0859319
dyskeratosis congenita, autosomal recessive 8 is a multisystem condition that primarily affects hematologic function, immune regulation, and developme...
MONDO:0031057
Dyskeratosis congenita, digenic is a multi-system condition that primarily affects the skin, hair, and immune system, with some individuals also exper...
MONDO:0010584
Dyskeratosis congenita, X-linked is a disorder affecting the skin, nails, and mucous membranes, with potential involvement of blood cell production an...
MONDO:0800028
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.