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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 6,341-6,360 of 10,888 diseases
MONDO:0009274
Ghosal hematodiaphyseal dysplasia is an extremely rare inherited condition primarily affecting the skeletal system and blood, characterized by abnorma...
MONDO:0000128
Giant axonal neuropathy is a rare inherited condition that affects the nervous system by disrupting the normal structure of neurofilaments, leading to...
MONDO:0009749
Giant axonal neuropathy 1 is a degenerative disorder affecting both the peripheral and central nervous systems. It is caused by pathogenic variants in...
MONDO:0012411
MONDO:0016682
Giant cell glioblastoma is a rare variant of glioblastoma, an aggressive brain tumor classified as WHO grade IV. This tumor is distinguished by the pr...
MONDO:1060166
Giant cell hepatitis with autoimmune hemolytic anemia is a rare autoimmune condition that typically presents in early childhood. This disorder is char...
MONDO:0023232
Giant cell myocarditis is an inflammatory disorder of the heart muscle that is associated with an aggressive autoimmune process. Recognized subtypes,...
MONDO:0006770
Giant cell reparative granuloma is a rare, tumor-like lesion that most often affects the hands and feet. It is characterized by hemorrhagic fibrous ti...
MONDO:0003643
Giant hemangioma is a cavernous hemangioma characterized by hyalinized vascular channels and is often associated with calcifications, fibrosis, and he...
MONDO:0007745
Gilbert syndrome is an inherited condition that is usually harmless. It is characterized by higher than normal levels of unconjugated bilirubin in the...
MONDO:0009890
Gillessen-Kaesbach-Nishimura syndrome is a rare genetic condition that is noted to include polycystic kidney disease along with distinct physical char...
MONDO:0005507
MONDO:0009228
MONDO:0007610
Gingival fibromatosis-hypertrichosis syndrome is a condition characterized by an abnormal overgrowth of the gums combined with excessive hair growth,...
MONDO:0007612
Gingival fibromatosis-progressive deafness syndrome is a condition where people experience an overgrowth of the gums (gingival fibromatosis) along wit...
MONDO:0850089
Information about overview is currently limited for this condition.
MONDO:0009904
Gitelman syndrome is an inherited electrolyte disorder primarily affecting renal function, characterized by hypokalemic metabolic alkalosis, significa...
MONDO:0035472
GJC2-related late-onset primary lymphedema is a rare genetic condition that mainly affects the lymphatic system. People with this condition develop ly...
MONDO:0005774
MONDO:0000320
Glandular tularemia, also known as lymph node tularemia, is an infection characterized by the involvement of lymph nodes. It is a clinical form of tul...
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