Rare Disease Index
9,491 diseasesrenal hypoplasia
kidney disease that is characterized by abnormally small kidneys with normal morphology and reduced number of nephrons
ICD: Q60.5
renal hypoplasia, bilateral
Bilateral renal hypoplasia is a form of renal hypoplasia (see this term), a renal developmental anomaly in which both kidneys are small and have a deficit in the number of nephrons present
renal hypoplasia, unilateral
Unilateral renal hypoplasia is a form of renal hypoplasia (see this term), a renal developmental anomaly in which one kidney is small and has a deficit in the number of nephrons present
Renal medullary carcinoma
medical condition
renal tubular dysgenesis
renal tubular dysgenesis due to twin-twin transfusion
renal tubular dysgenesis of genetic origin
instance of renal tubular dysgenesis that is caused by a modification of the individual's genome
renal-genital-middle ear anomalies
human disease
MeSH: C564849
renal-hepatic-pancreatic dysplasia
physical disorder characterized by pancreatic fibrosis, renal dysplasia and hepatic dysgenesis; it is usual fatal soon after birth
Renier-Gabreels-Jasper syndrome
Renin-angiotensin-aldosterone system-blocker-induced angioedema
Renin-angiotensin-aldosterone system (RAAS)-blocker induced angioedema (RAE) is a type of acquired angioedema (AAE, see this term) characterized by acute edema in subcutaneous tissues, viscera and/or the upper airway
Renpenning syndrome
intellectual disability that is characterized by small head size (microcephaly), long narrow face, short stature, small testes, and intellectual deficit which follows X-linked inheritance and presents most often in males
MeSH: C537761
resistance to thyrotropin-releasing hormone syndrome
Respiratory bronchiolitis interstitial lung disease
medical condition
respiratory or mediastinal malformation
human disease
respiratory or thoracic malformation
human disease
respiratory system abnormality
congenital structural abnormality of the respiratory system
ICD: Q34.9MeSH: D015619
respiratory system cancer
organ system cancer located in the respiratory system that is characterized by uncontrolled cellular proliferation in the respiratory tract
ICD: C32
restrictive cardiomyopathy
form of cardiomyopathy in which the walls are rigid,and the heart is restricted from stretching and filling with blood properly
MeSH: D002313
restrictive dermopathy
human disease
MeSH: C536920
reticular dysgenesis
Human disease
ICD: D81.0MeSH: C538361
reticular dystrophy of retinal pigment epithelium
human disease
reticular perineurioma
human disease
reticulate acropigmentation of Kitamura
Human disease
MeSH: C562924
Retiform hemangioendothelioma
intermediate, locally aggressive and rarely metastasizing blood vessel neoplasm. It is characterized by the presence of hobnail endothelial cells and formation of arborizing vascular channels
retinal arterial tortuosity
human disease
retinal degeneration-nanophthalmos-glaucoma syndrome
MeSH: C538364
retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
human disease
retinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome
MeSH: C535283
retinal macular dystrophy type 2
human disease