Trusted information across 10,888 rare diseases — plain language, always cited, free for everyone.
Can't find your disease? Try searching by gene, symptom, or OMIM ID.
Every report passes a 3-tier quality pipeline with gene validation, fact-checking, and safety checks.
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and more. Every claim is cited.
Data syncs range from 3x daily (news) to weekly (trials, FDA). Reports regenerate when data changes.
Showing 8,221-8,240 of 10,888 diseases
MONDO:0009090
Hearing loss, sensorineural, autosomal-mitochondrial type is a condition that primarily affects the auditory system, leading to sensorineural hearing...
MONDO:0017921
Hearing loss-familial salivary gland insensitivity to aldosterone syndrome is a condition marked by bilateral moderate-to-severe sensorineural hearing...
MONDO:0009008
MONDO:0008917
Heart defects-limb shortening syndrome is a condition characterized by the co-occurrence of congenital heart malformations and skeletal dysplasia, inc...
MONDO:0005267
Heart disorder is a condition involving the heart and/or the pericardium that primarily affects the cardiac system. While the disorder can manifest in...
MONDO:0003742
Heart fibrosarcoma is an aggressive malignant tumor arising from the heart, characterized by a distinct herringbone growth pattern of spindle-shaped f...
MONDO:0003353
Heart leiomyosarcoma is an aggressive malignant tumor arising from the smooth muscle cells of the heart. It is classified as a cardiac tumor and is ch...
MONDO:0003917
MONDO:0003354
Heart sarcoma is a malignant tumor of the heart, most often presenting as an angiosarcoma. This condition affects the cardiac tissue and can disrupt n...
MONDO:0009327
Heart, malformation of refers to structural abnormalities of the heart that are present at birth. This condition typically affects the heart’s anatomy...
MONDO:0016432
Heart-hand syndrome, also known as atriodigital dysplasia, represents a group of congenital conditions characterized by malformations affecting both t...
MONDO:0015284
MONDO:0007702
MONDO:0012417
MONDO:0019728
Heavy chain deposition disease (HCDD) is a disorder characterized by abnormal deposits of immunoglobulin heavy chains in body tissues, most affecting...
MONDO:0019464
Heavy chain disease is a rare lymphoplasma-cell proliferative disorder in which B cells produce truncated immunoglobulin heavy chains without associat...
MONDO:0023305
MONDO:0007176
Helicoid peripapillary chorioretinal degeneration is an inherited condition that affects the retina and choroid of the eye, often leading to progressi...
MONDO:0016748
Hemangioblastoma is a rare, benign tumor that arises within the central nervous system, most commonly in the cerebellum or spinal cord. It is a highly...
MONDO:0006557
Hemangioma of subcutaneous tissue is a benign growth arising from the soft tissues beneath the skin. It is categorized as a vascular anomaly that typi...
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