Disease Index
9,486 diseasesqualitative or quantitative defects of TRIM32
human disease
qualitative or quantitative defects of tropomyosin
human disease
qualitative or quantitative defects of troponin
human disease
qualitative or quantitative protein defects in neuromuscular diseases
human disease
quantitative and/or qualitative congenital phagocyte defect
human disease
rabies
deadly viral disease, transmitted through animals
MeSH: D011818
Rabson–Mendenhall syndrome
medical condition
ICD: E13
Radial aplasia
congenital defect which affects the formation of the radius bone in the arm
radial deficiency-tibial hypoplasia syndrome
human disease
radial dysplasia
radial hemimelia is a congenital longitudinal deficiency of the radius bone of the forearm characterized by partial or total absence of the radius
radial hemimelia, bilateral
human disease
radial hemimelia, unilateral
human disease
radial ray hypoplasia-choanal atresia syndrome
Radial ray hypoplasia - choanal atresia is an extremely rare syndrome characterized by radial ray hypoplasia, choanal atresia and convergent strabismus
MeSH: C536263
radiation myelitis
disease characterized by white matter damage to the spinal cord developed after a certain period of application of ionizing radiation
Radiation proctitis
Swelling of blood vessels of rectum/colon post radiation.
ICD: K62.7
radiation syndrome
health problems caused by exposure to very high levels of ionizing radiation
ICD: T66MeSH: D054508
radio-renal syndrome
medical condition
MeSH: C536267
radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome
gene (7p15)
radio-ulnar synostosis, bilateral
human disease
radio-ulnar synostosis, unilateral
human disease
radioulnar synostosis
Human disease
MeSH: C562408
radioulnar synostosis with amegakaryocytic thrombocytopenia 1
human disease
radioulnar synostosis-developmental delay-hypotonia syndrome
MeSH: C538217
Raine syndrome
Lethal osteosclerotic bone dysplasia is defined by generalized osteosclerosis with periosteal bone formation, characteristic facial dysmorphism, brain abnormalities including intracerebral calcifications, and neonatal lethal course
MeSH: C535282
Ramon syndrome
human disease
MeSH: C535285
Ramos-Arroyo syndrome
medical condition
MeSH: C535286
rapadilino 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