Rare Disease Index
9,491 diseasesrapadilino syndrome
Human disease
ICD: Q87.1MeSH: C535288
Rapidly involuting congenital hemangioma
rapidly progressive glomerulonephritis
human disease
Rapp-Hodgkin syndrome
autosomal dominant disease characterized by abnormal development of ectodermal tissues including the skin, hair, nails, teeth and sweat glands and anhidrotic ectodermal dysplasia with cleft lip/palate
MeSH: C535289
rare abdominal surgical disease
human disease
rare acquired eye disease
human disease
rare adenocarcinoma of the breast
Any of the forms of breast adenocarcinoma that have a rare incidence
rare adrenal disease
human disease
rare adult hypothyroidism
human disease
rare allergic disease
rare allergic hypersensitivity disease
rare allergic respiratory disease
rare respiratory allergy
rare anemia
Rare anemia
rare autonomic nervous system disorder
Rare autonomic nervous system disease
rare bone disease
type of disease
rare bone disease related to a common gene or pathway defect
human disease
rare breast tumor
rare bronchopulmonary tumor
human disease
rare cancer of corpus uteri
human disease
rare capillary malformation with associated anomalies
human disease
rare cardiac disease
rare heart disease
rare cause of hypertension
human disease
rare circulatory system disease
rare form of cardiovascular disease
rare combined vascular malformation
human disease
rare constitutional hemolytic anemia due to an enzyme disorder
human disease
rare cutaneous lichen planus
human disease
rare deafness
any of the forms of hearing loss that have a rare incidence
rare developmental defect with connective tissue involvement
human disease
Rare diabetes mellitus
human disease
rare disease
disease that affects a small percentage of the population
MeSH: D035583
rare disease involving intestinal motility
human disease