Rh incompatibility - A condition in which a pregnant woman with Rh-negative blood is exposed to Rh-positive blood cells (usually from the fetus). Inclusion on this list does not serve as official recognition by the NIH that a disease is rare. Rare NSID - Another name for Rare intellectual disability without developmental anomaly Rare tumor of cranial and spinal nerves - See Tumor of cranial and spinal nerves; Rare tumor of liver and intrahepatic biliary tract - See Primary liver cancer; RARS - See Sideroblastic anemia pyridoxine-refractory autosomal recessive; Rasmussen encephalitis Ringworm - Fungal infection in the form of a red, scaly, itchy patch or bump. This list includes the main name for each condition, as well as alternate names. Get the latest public health information from CDC: No hemos publicado información en español sobre enfermedades que comiencen con esta letra. Some conditions that are not Radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopeniaRadial-ulnar hypoplasia with bone marrow failure and/or leukemiaRadioulnar synostosis and a typical rhomboid shape of the tibia and fibulaRaphe, supraumbilical midline, with cavernous facial hemangiomasRapidly progressive glomerulonephritis with pulmonary hemorrhageRapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulationRare intellectual disability without developmental anomalyRecessive dystrophic epidermolysis bullosa, generalized intermediateRecessive dystrophic epidermolysis bullosa, non-Hallopeau-Siemens typeRecessive dystrophic epidermolysis bullosa, severe generalizedRecessive spastic paraplegia with retinal degenerationRecurrent infection due to specific granule deficiencyRecurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndromeRecurrent spontaneous hypothermia with hypoplasia of the corpus callosumRelapsing febrile nodular nonsuppurative panniculitisRenal and craniofacial anomalies with persistence of mullerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactylyRenal dysplasia or hydronephrosis, oligohydramnios and subsequent lung hypoplasia due to urethral obstructionRenal dysplasia, mesomelia, and radiohumeral fusionRenal Fanconi syndrome with nephrocalcinosis and renal stonesRenal hamartomas, nephroblastomatosis, and fetal gigantismRenal tubular acidosis with progressive nerve deafnessRenal tubular acidosis, autosomal recessive with preserved hearingRenal tubular acidosis, autosomal recessive, with progressive nerve deafnessRENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE, WITH LATE-ONSET SENSORINEURAL HEARING LOSS, INCLUDEDRENAL TUBULAR ACIDOSIS, DISTAL, WITH NORMAL RED CELL MORPHOLOGY, INCLUDEDRenal tubular acidosis, distal, with progressive nerve deafnessRenal-hepatic-pancreatic dysplasia-Dandy-Walker cysts syndromeREN-associated familial juvenile hyperuricemic nephropathyRetarded growth, hydrocephalus, micrognathia, intestinal malrotation, omphalocele, short lower limbs and foot deformitiesRetention of dietary cholesterol and abnormal retention of non-cholesterol sterols in the bodyReticular skin changes, dental anomalies, decreased function of sweat glands, strabismus, and optic atrophyRetinal arterial macroaneurysm and supravalvular pulmonic stenosisRetinal degeneration, autosomal recessive, prominin-relatedRetinal degeneration, late-onset, autosomal dominant Retinal detachment-occipital encephalocele syndromeRetinal pigmentary degeneration, microcephaly, and severe mental retardationRetinal telangiectasia associated with hypogammaglobulinemiaRetinal vasculopathy and cerebral leukoencephalopathyRetinal vasculopathy and cerebral leukoencephalopathyRetinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsRetinal vasculopathy with cerebral leukoencephalopathy and systemic manifestationsRetinitis pigmentosa and intellectual disability due to del(X)(p11.3)Retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletionRetinitis pigmentosa, HYpopituitarism, Nephronophthisis, and mild Skeletal dysplasiaRetinitis pigmentosa-intellectual disability- labyrinthine deafness-hypogenitalism syndromeRetinitis pigmentosa-intellectual disability-sensorineural hearing loss-hypogenitalism syndromeRetinopathy, vascular, with cerebral and renal involvement and Raynaud and migraine phenomenaRheumatoid factor negative erosive chronic polyarthritisRHOBTB2-related developmental and epileptic encephalopathyRibonucleic acid polymerase III-related leukodystrophyRichieri-Costa and Pereira form of acrofacial dysostosisRight bundle branch block, ST segment elevation, and sudden death syndromeRitscher-Schinzel cranio-cerebello-cardiac syndromeRobin sequence with cleft mandible and limb anomaliesRound face with depressed nasal bridge and small mouth, congenital heart defect, and retarded developmentRutledge lethal multiple congenital anomaly syndrome Por favor If you have problems viewing PDF files, download the latest version of Genetic and Rare Diseases Information Center (GARD) - PO Box 8126, Gaithersburg, MD 20898-8126 - Toll-free: 1-888-205-2311Browse the GARD list of rare diseases and related terms to find topics of interest to you. Rickettsial Diseases; Rickettsia rickettsii Infection — see Rocky Mountain Spotted Fever; Rift Valley Fever (RVF) Ringworm from Animals; Ringworm [Dermatophyte Infection] River Blindness [Onchocerciasis] RMSF (Rocky Mountain Spotted Fever) Rocky Mountain Spotted Fever (RMSF) [Rickettsia rickettsii Infection] Rodent Control — see Rodents, Diseases from Long-term survival for children with advanced disease older than 18 months of age is poor and most of the

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