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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 7,161-7,180 of 10,888 diseases
MONDO:0015548
Information about the overall nature of Huntington disease-like syndrome is currently limited for this condition. This condition is also known as Hunt...
MONDO:0018425
Huntington disease-like syndrome due to C9ORF72 expansions is a rare condition that shares some features with Huntington disease. It is sometimes refe...
MONDO:0013772
Huppke-Brendel syndrome is a rare disorder that has been reported under several names, including acetyl CoA transporter deficiency and congenital cata...
MONDO:0011759
Hurler-Scheie syndrome is a rare lysosomal storage disease. It is an intermediate form of mucopolysaccharidosis type 1 (MPS1), positioned between Hurl...
MONDO:0011758
Hurler syndrome is the most severe form of mucopolysaccharidosis type 1 (MPS I), a lysosomal storage disorder that affects multiple organ systems incl...
MONDO:0008310
Hutchinson-Gilford progeria syndrome is a very rare, life-limiting disorder characterized by features of premature aging that become evident in early...
MONDO:0018889
MONDO:0009229
Hyaline fibromatosis syndrome is a very rare inherited condition that affects multiple systems including the skeletal, skin, and gastrointestinal syst...
MONDO:0044138
MONDO:0006248
Hydatidiform mole is a gestational trophoblastic disorder in which the chorionic villi grow abnormally, leading to an enlarged uterus and other pregna...
MONDO:0009273
Hydatidiform mole, recurrent, 1 is a condition in which abnormal growth of placental tissue occurs during pregnancy. It is caused by mutations in the...
MONDO:0013671
Hydatidiform mole, recurrent, 2 is a condition characterized by the development of abnormal trophoblastic tissue in the uterus due to a mutation in th...
MONDO:0032746
Hydatidiform mole, recurrent, 3 is an inherited condition primarily affecting reproductive health, manifesting as abnormal molar growth in the uterus...
MONDO:0032747
Hydatidiform mole, recurrent, 4 is a disorder of the reproductive system that involves abnormal placental development and is a recognized cause of fem...
MONDO:0016344
MONDO:0018024
Hydroa vacciniforme is a rare photodermatitis that predominantly affects children and is characterized by the development of vesicular lesions and sca...
MONDO:0011371
Hydroa vacciniforme, familial is an inherited skin condition characterized by episodes of sun-induced lesions that can leave scar-like marks resemblin...
MONDO:0018224
Hydroa vacciniforme-like lymphoma is a rare, Epstein-Barr virus-positive cutaneous T-cell lymphoproliferative disorder that primarily affects children...
MONDO:0016350
MONDO:0054794
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.