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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 6,221-6,240 of 10,888 diseases
MONDO:0030476
Galloway-Mowat syndrome 10 (also known as GAMOS10) is a rare genetic condition. Although detailed information about this disorder is limited, it is kn...
MONDO:0033006
Galloway-Mowat syndrome 2, X-linked is a rare genetic condition. It is also known by several names including GAMOS2 and X-linked recessive. Detailed i...
MONDO:0033007
Galloway-Mowat syndrome 3 (also known as GAMOS3) is a rare genetic condition that has been identified by its association with the OSGEP gene. It is ca...
MONDO:0033008
Information about overview is currently limited for this condition.
MONDO:0033009
Galloway-Mowat syndrome 5 (GAMOS5) is a rare condition that has been recognized in scientific databases with the identifier OMIM:617731. While detaile...
MONDO:0032691
Galloway-Mowat syndrome 6, also known as GALLOWAY-MOWAT SYNDROME 6 or GAMOS6, is a rare condition with very limited publicly available information. It...
MONDO:0032692
Galloway-Mowat syndrome 7, also known as GAMOS7, is a rare genetic condition that has been linked to changes in the NUP107 gene. Detailed clinical inf...
MONDO:0032693
Galloway-Mowat syndrome 8 (GAMOS8) is a rare genetic condition that has been linked to changes in the NUP133 gene. This condition is identified in rec...
MONDO:0030471
Galloway-Mowat syndrome 9 (also known as GAMOS9) is a rare genetic condition that has been associated with changes in the GON7 gene. It is recognized...
MONDO:0000698
Gamma-amino butyric acid metabolism disorder is an amino acid metabolic condition characterized by impairment of the GABA catabolic pathway. Variants...
MONDO:0009259
Gamma-glutamylcysteine synthetase deficiency is a very rare inherited metabolic disorder that primarily affects the red blood cells, leading to hemoly...
MONDO:0009285
Gamma-glutamyl transpeptidase deficiency is a metabolic condition characterized by abnormally high levels of glutathione in both the plasma and urine....
MONDO:0015046
Gamma-heavy chain disease is a rare hematologic disorder characterized by the production of incomplete monoclonal gamma-heavy chains without accompany...
MONDO:0007646
Gamstorp-Wohlfart syndrome is a rare condition that affects the peripheral nerves. It is a slowly progressive disorder in which the nerve fibers, espe...
MONDO:0016730
Gangliocytoma, also known as GNC, is a well differentiated, slow-growing neuroepithelial neoplasm composed of mature ganglion cells that most commonly...
MONDO:0016733
Ganglioglioma is a well‐differentiated, slow growing neoplasm of the central nervous system that exhibits both neuronal and glial features. It is clas...
MONDO:0005035
Ganglioneuroblastoma is a malignant neuroblastic tumor that is characterized by the presence of neuroblastic cells, ganglion cells, and a stroma with...
MONDO:0005033
Ganglioneuroma is a benign neuroblastic tumor that arises from the sympathetic nervous system, most commonly from the sympathetic trunk in the mediast...
MONDO:0017719
Gangliosidosis refers to a group of autosomal recessive lysosomal storage disorders characterized by the abnormal accumulation of gangliosides due to...
MONDO:0009263
GAPO syndrome is a rare condition that affects several parts of the body. It is known as a multiple congenital anomalies (MCA) syndrome that involves...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.