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Rare Disease Intelligence — 10,888 conditions monitored | Kisho | Kisho

Open data · 12 authoritative sources

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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.

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12

authoritative sources — clinical, regulatory, scientific

10,888

rare conditions, continuously monitored

Daily

updates from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet…

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Showing 5,021-5,040 of 10,888 diseases

duodenal neuroendocrine tumor, well differentiated, low or intermediate grade

MONDO:0015063

Duodenal neuroendocrine tumor, well differentiated, low or intermediate grade is a type of tumor arising from the neuroendocrine cells in the duodenum...

duodenal somatostatinoma

MONDO:0004236

Duodenal somatostatinoma is a neuroendocrine tumor that arises in the duodenum and produces the hormone somatostatin. It is characterized by the prese...

duodenum cancer

MONDO:0000920

Duodenum cancer is a malignant tumor that affects the duodenum, a critical part of the small intestine. This condition can present as different types...

duplication/inversion 15q11

MONDO:0018027

Duplication/inversion 15q11, also known as isodicentric chromosome 15 syndrome, is a chromosomal abnormality in which an extra copy of chromosome 15 m...

duplication of the pituitary gland

MONDO:0017808

Duplication of the pituitary gland, also known as DPG-plus syndrome, is an extremely rare developmental anomaly affecting the structure of the pituita...

duplication of urethra

MONDO:0016529

Duplication of the urethra, also known as urethral duplication, is a rare congenital anomaly affecting the genitourinary system. This condition encomp...

dural sinus malformation

MONDO:0019972

Dural sinus malformation is a vascular condition affecting the venous channels of the brain, often characterized by abnormal connections between arter...

Dyggve-Melchior-Clausen disease

MONDO:0009130

Dyggve-Melchior-Clausen disease is a rare skeletal disorder that belongs to a group known as spondyloepimetaphyseal dysplasias. This condition affects...

Dyggve-Melchior-Clausen syndrome, X-linked

MONDO:0010583

Dyggve-Melchior-Clausen syndrome, X-linked is a rare inherited condition. This form is described as the X-linked form of Dyggve-Melchior-Clausen disea...

dyneinopathy

MONDO:1040031

Dyneinopathy refers to a spectrum of disorders that impact both the neuromuscular system and neurodevelopment. Affected individuals may experience mus...

DYRK1A-related intellectual disability syndrome

MONDO:0013578

DYRK1A-related intellectual disability syndrome is a very rare condition that primarily affects neurodevelopment, resulting in severe intellectual dis...

DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion

MONDO:0017056

DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion is a rare genetic condition that involves the loss of a small piece...

dysbaric osteonecrosis

MONDO:0000840

Dysbaric osteonecrosis is a form of avascular necrosis characterized by the death of bone tissue, believed to result from nitrogen embolism, often ass...

dyschondrosteosis-nephritis syndrome

MONDO:0007482

Dyschondrosteosis-nephritis syndrome is a condition characterized by distinctive skeletal abnormalities in conjunction with kidney involvement. Affect...

dyschromatosis symmetrica hereditaria

MONDO:0007483

Dyschromatosis symmetrica hereditaria is a skin disorder characterized by a mixture of hyperpigmented and hypopigmented macules that primarily affect...

dyschromatosis universalis hereditaria

MONDO:0000736

Dyschromatosis universalis hereditaria is a pigmentation disorder characterized by a generalized pattern of both hyperpigmented and hypopigmented macu...

dyschromatosis universalis hereditaria 1

MONDO:0024524

Dyschromatosis universalis hereditaria 1 is a genetic skin condition marked by differences in skin pigmentation. Although detailed characteristic find...

dyschromatosis universalis hereditaria 2

MONDO:0012993

Dyschromatosis universalis hereditaria 2 (DUH2) is a condition characterized by irregular skin pigmentation, where affected individuals develop both l...

dyschromatosis universalis hereditaria 3

MONDO:0014169

Dyschromatosis universalis hereditaria 3 is a condition characterized by abnormal skin pigmentation, in which affected individuals develop patches of...

dysembryoplastic neuroepithelial tumor

MONDO:0005505

Dysembryoplastic neuroepithelial tumor is a benign glial-neuronal neoplasm that primarily affects children and young adults. It is most commonly locat...

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