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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 8,941-8,960 of 10,888 diseases
MONDO:0006835
MONDO:0009530
Lipoid proteinosis is a rare genodermatosis that primarily affects the skin and mucous membranes, with early signs including a hoarse voice that typic...
MONDO:0007907
Lipoma of the conjunctiva is a benign growth that involves the fatty tissue of the eye’s conjunctival surface. While the condition is generally consid...
MONDO:0970960
MONDO:0012296
Lipomyelomeningocele is a neural tube closure defect that presents as a subcutaneous lipoma extending through a defect in the lower spine, usually in...
MONDO:0012725
MONDO:0005060
Liposarcoma is a malignant tumor that arises from adipose tissue and is typically painless. It presents as a mass that may be discovered incidentally...
MONDO:0002634
Liposarcoma of bone is a very rare malignant tumor originating from adipose tissue within the bone. This condition falls under the category of maligna...
MONDO:0003589
Liposarcoma of the ovary is a malignant tumor that arises from adipose (fat) tissue within the ovary. As an ovarian neoplasm, it is categorized among...
MONDO:0014576
Lipoyl transferase 1 deficiency is a very rare metabolic disorder that primarily affects the central nervous system. It results from pathogenic varian...
MONDO:0010425
Lisch epithelial corneal dystrophy (LECD) is a very rare disorder that affects the surface of the cornea, the clear front part of the eye. It is marke...
MONDO:0030031
MONDO:0013527
MONDO:0014534
MONDO:0014596
Lissencephaly 7 with cerebellar hypoplasia is a congenital brain malformation characterized by a smooth cerebral surface and underdevelopment of the c...
MONDO:0014992
Lissencephaly 8 is a neurodevelopmental condition characterized by an abnormal brain structure resulting from mutations in the TMTC3 gene. The disorde...
MONDO:0032677
MONDO:0011830
Lissencephaly due to LIS1 mutation is a brain malformation that affects the cerebral cortex, leading to a smooth brain surface and abnormal brain stru...
MONDO:0012703
Lissencephaly due to TUBA1A mutation is a congenital brain development disorder characterized by abnormal neuronal migration and disordered brain laye...
MONDO:0018838
Lissencephaly spectrum disorders refer to a group of congenital brain malformations characterized by a simplified or absent pattern of cerebral convol...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.