Browse A-Z | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program R/1 ENGLISH

Browse A-Z | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program





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Browse the GARD list of rare diseases and related terms to find topics of interest to you. This list includes the main name for each condition, as well as alternate names. Inclusion on this list does not serve as official recognition by the NIH that a disease is rare. Some conditions that are not considered rare are on this list and are labeled accordingly.Read more about which diseases are included on the GARD website.

• R1 - See Ring chromosome 1
• R10 - See Ring chromosome 10
• R11 - See Ring chromosome 11
• R12 - See Ring chromosome 12
• R13 - See Ring chromosome 13
• R15 - See Ring chromosome 15
• R16 - See Ring chromosome 16
• R17 - See Ring chromosome 17
• R18 - See Ring chromosome 18
• R19 - See Ring chromosome 19
• R2 - See Ring chromosome 2
• R20 - See Ring chromosome 20
• R21 - See Ring chromosome 21
• R22 - See Ring chromosome 22
• R3 - See Ring chromosome 3
• R4 - See Ring chromosome 4
• R5 - See Ring chromosome 5
• R6 - See Ring chromosome 6
• R7 - See Ring chromosome 7
• R8 - See Ring chromosome 8
• R9 - See Ring chromosome 9
• Rabbit fever - See Tularemia
• Rabies
• Rabson-Mendenhall syndrome
• Rachischisis - See Spina bifida
• Radial and patellar aplasia - See Rapadilino syndrome
• Radial and patellar hypoplasia - See Rapadilino syndrome
• Radial aplasia, X-linked - See Radius absent anogenital anomalies
• Radial defect Robin sequence
• Radial hypoplasia triphalangeal thumbs hypospadias maxillary diastema - See Schmitt Gillenwater Kelly syndrome
• Radial hypoplasia, triphalangeal thumbs and hypospadias
• Radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema - See Radial hypoplasia, triphalangeal thumbs and hypospadias
• Radial ray agenesis
• Radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia - See IVIC syndrome
• Radial ray hypoplasia and choanal atresia - See Radial ray hypoplasia choanal atresia
• Radial ray hypoplasia choanal atresia
• Radial-ulnar hypoplasia with bone marrow failure and/or leukemia - See WT limb blood syndrome
• Radial-ulnar synostosis - See Congenital radioulnar synostosis
• Radiation induced angiosarcoma of the breast
• Radiation induced brachial neuritis - See Radiation induced brachial plexopathy
• Radiation induced brachial plexopathy
• Radiation induced cancer
• Radiation induced meningioma
• Radiation injury to the brachial plexus - See Radiation induced brachial plexopathy
• Radiation related cancer - See Radiation induced cancer
• Radicular dentin dysplasia - See Dentin dysplasia, type 1
• Radio renal syndrome
• Radio-digito-facial dysplasia
• Radio-renal syndrome - See Radio renal syndrome
• Radioulnar synostosis - See Congenital radioulnar synostosis
• Radio-ulnar synostosis - See Congenital radioulnar synostosis
• Radioulnar synostosis and a typical rhomboid shape of the tibia and fibula - See Nievergelt syndrome
• Radio-ulnar synostosis type 1 - See Congenital radioulnar synostosis
• Radio-ulnar synostosis type 2 - See Congenital radioulnar synostosis
• Radioulnar synostosis-microcephaly-scoliosis syndrome
• Radius absent anogenital anomalies
• RAE - See Reactive angioendotheliomatosis
• RAEB - See Myelodysplastic Syndrome With Excess Blasts
• RAF1 gene related Noonan syndrome - See Noonan syndrome
• Ragpicker's disease - See Anthrax
• Rahman syndrome
• Raine syndrome
• Rambam-Hasharon syndrome - See SLC35C1-CDG (CDG-IIc)
• Ramer Ladda syndrome
• Ramon Syndrome
• Ramos Arroyo Clark syndrome
• Ramos-Arroyo syndrome - See Ramos Arroyo Clark syndrome
• Ramsay Hunt cerebellar syndrome - See Dyssynergia cerebellaris myoclonica
• Ramsay Hunt syndrome - See Herpes zoster oticus
• Ramsay Hunt syndrome type 1 (formerly) - See Dyssynergia cerebellaris myoclonica
• Ramsay Hunt syndrome type 2 (formerly) - See Herpes zoster oticus
• RAMSVPS - See Retinal arterial macroaneurysm with supravalvular pulmonic stenosis
• Rapadilino syndrome
• Raphe, supraumbilical midline, with cavernous facial hemangiomas - See Supraumbilical midabdominal raphe and facial cavernous hemangiomas
• Rapidly progressive glomerulonephritis with pulmonary hemorrhage - See Goodpasture syndrome
• Rapid-onset dystonia-parkinsonism
• Rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation - See ROHHAD
• Rapp-Hodgkin ectodermal dysplasia syndrome - See Rapp-Hodgkin syndrome
• Rapp-Hodgkin syndrome
• Rare adenocarcinoma of the breast
• Rare bone tumor - See Primary bone cancer
• Rare form of Hirschsprung's disease - See Aganglionosis, total intestinal
• Rare intellectual disability without developmental anomaly
• Rare lichen planus
• Rare LP - See Rare lichen planus
• Rare non-syndromic intellectual deficiency - Another name for Rare intellectual disability without developmental anomaly
• Rare non-syndromic intellectual disability - Another name for Rare intellectual disability without developmental anomaly
• 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
• Rasmussen Johnsen Thomsen syndrome
• Rasmussen syndrome - See Rasmussen Johnsen Thomsen syndrome
• Rat bite fever
• Rathburn disease - See Hypophosphatasia
• Rathke's pouch tumor - See Craniopharyngioma
• RB - See Retinoblastoma
• RBCD - See Corneal dystrophy of Bowman layer type 1
• RBS - See Roberts syndrome
• RCAD - See Maturity-onset diabetes of the young
• RCC4 - See Renal cell carcinoma 4
• RCCP - See Papillary renal cell carcinoma
• RCD1 - See Retinal cone dystrophy 1
• RCD2 - See Retinal cone dystrophy 2
• RCD3A - See Retinal cone dystrophy 3A
• RCD3B - See Retinal cone dystrophy 3B
• RCD4 - See Retinal cone dystrophy 4
• RCDP - See Rhizomelic chondrodysplasia punctata
• RCDP1 - See Rhizomelic chondrodysplasia punctata type 1
• RCDP2 - See Rhizomelic chondrodysplasia punctata
• RCDP3 - See Rhizomelic chondrodysplasia punctata
• RCL - See Abdominal cystic lymphangioma
• RCRD2 - See Cone-rod dystrophy 2
• RCUD - See Refractory cytopenia with unilineage dysplasia
• RCVS - See Reversible cerebral vasoconstriction syndrome
• RD - See Reticular dysgenesis
• RDC - See Ring dermoid of cornea
• RDD - See Rosai-Dorfman disease
• RDEB generalisata gravis - See Severe generalized recessive dystrophic epidermolysis bullosa
• RDEB generalisata mitis - See Recessive dystrophic epidermolysis bullosa-generalized other
• RDEB, generalized intermediate - See Recessive dystrophic epidermolysis bullosa-generalized other
• RDEB, Hallopeau-Siemens type - See Severe generalized recessive dystrophic epidermolysis bullosa
• RDEB, non-Hallopeau-Siemens type - See Recessive dystrophic epidermolysis bullosa-generalized other
• RDEB, severe generalized - See Severe generalized recessive dystrophic epidermolysis bullosa
• RDEB-generalized other - See Recessive dystrophic epidermolysis bullosa-generalized other
• RDEB-O - See Recessive dystrophic epidermolysis bullosa-generalized other
• RDEB-sev gen - See Severe generalized recessive dystrophic epidermolysis bullosa
• RDP - See Rapid-onset dystonia-parkinsonism
• RDPA - See Refsum disease with increased pipecolic acidemia
• RDS - infants - See Respiratory distress syndrome, infant
• RE - See Rasmussen encephalitis
• Reactive angioendotheliomatosis
• Reactive arthritis
• REAR syndrome - See Townes-Brocks syndrome
• Reardon Wilson Cavanagh syndrome
• Reardon-Hall-Slaney syndrome - See Mesomelic dwarfism cleft palate camptodactyly
• Rec8 syndrome - See Recombinant chromosome 8 syndrome
• Recessive aplasia cutis congenita of the limbs - See Aplasia cutis congenita of limbs recessive
• Recessive ataxia of Beauce - See Spinocerebellar ataxia autosomal recessive 8
• Recessive dystrophic epidermolysis bullosa - See Dystrophic epidermolysis bullosa
• Recessive dystrophic epidermolysis bullosa, generalized intermediate - See Recessive dystrophic epidermolysis bullosa-generalized other
• Recessive dystrophic epidermolysis bullosa, non-Hallopeau-Siemens type - See Recessive dystrophic epidermolysis bullosa-generalized other
• Recessive dystrophic epidermolysis bullosa, severe generalized - See Severe generalized recessive dystrophic epidermolysis bullosa
• Recessive dystrophic epidermolysis bullosa-generalized other
• Recessive microcephaly with spastic quadriplegia - See Microcephaly with spastic quadriplegia
• Recessive pseudoachondroplasia - See Pseudoachondroplastic dysplasia 2
• Recessive spastic paraplegia with retinal degeneration - See Spastic paraplegia 15
• Recklinghausen's disease - See Neurofibromatosis type 1
• Recombinant chromosome 8 syndrome
• Rectal cancer, childhood
• Recurrent acute necrotizing encephalopathy - See Infection-induced acute encephalopathy 3
• Recurrent duplication of 17q12 - See 17q12 duplication
• Recurrent familial intrahepatic cholestasis 1 - See Benign recurrent intrahepatic cholestasis 1
• Recurrent familial intrahepatic cholestasis 2 - See Benign recurrent intrahepatic cholestasis 2
• Recurrent hydatidiform mole
• Recurrent infection due to specific granule deficiency - See Neutrophil-specific granule deficiency
• Recurrent intrahepatic cholestasis of pregnancy - See Intrahepatic cholestasis of pregnancy
• Recurrent laryngeal papillomatosis (subtype) - See Laryngeal papillomatosis
• Recurrent meningitis - See Mollaret meningitis
• Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome - See TANGO2-Related Metabolic Encephalopathy and Arrhythmias
• Recurrent peripheral facial palsy
• Recurrent polychondritis - See Relapsing polychondritis
• Recurrent polyserositis - See Familial Mediterranean fever
• Recurrent respiratory papillomatosis
• Recurrent Scarring Aphthae - See Sutton disease 2
• Recurrent spontaneous hypothermia with hypoplasia of the corpus callosum - See Shapiro syndrome
• Recurrent trigger thumb (type) - See Trigger thumb
• Red cell aldolase deficiency - See Glycogen storage disease type 12
• Red cell aplasia, pure hereditary - See Diamond-Blackfan anemia
• Red cell phospholipid defect with hemolysis
• Red skin pigment anomaly of New Guinea
• Red skin pigment, New Guinea type - See Red skin pigment anomaly of New Guinea
• Reducing body myopathy
• Reductional transverse limb defects
• Reed's syndrome - See Hereditary leiomyomatosis and renal cell cancer
• Reese retinal dysplasia
• Refetoff syndrome - See Generalized resistance to thyroid hormone
• Reflex sympathetic dystrophy - See Complex regional pain syndrome
• Refractory anemia with excess blasts - See Myelodysplastic Syndrome With Excess Blasts
• Refractory anemia with ringed sideroblasts - See Sideroblastic anemia pyridoxine-refractory autosomal recessive
• Refractory cytopenia with unilineage dysplasia
• Refractory macrocytic anemia due to 5q deletion - See 5q- syndrome
• Refrigeration palsy - See Bell's palsy
• Refsum disease
• Refsum disease with increased pipecolic acidemia
• Refsum disease, infantile form
• Reginato Shiapachasse syndrome
• Regional choroidal atrophy and alopecia - See Moloney syndrome
• Regressive metaphyseal dysplasia - See Metaphyseal anadysplasia
• Reifenstein syndrome, partial - See Partial androgen insensitivity syndrome
• Reis Bucklers corneal dystrophy - See Corneal dystrophy of Bowman layer type 1
• Reis Bucklers dystrophy - See Corneal dystrophy of Bowman layer type 1
• Reiter syndrome - See Reactive arthritis
• Reiter's syndrome - See Reactive arthritis
• Relapsing polychondritis
• Remitting seronegative symmetrical synovitis with pitting edema
• Remnant removal disease - See Hyperlipidemia type 3
• Renal adenocarcinoma - See Papillary renal cell carcinoma
• Renal adysplasia dominant type
• Renal agenesis
• Renal agenesis meningomyelocele mullerian defect
• Renal and anogenital malformations with syndactyly - See Green Sandford Davison syndrome
• Renal and craniofacial anomalies with persistence of mullerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly - See Persistence of mullerian derivatives with lymphangiectasia and postaxial polydactyly
• Renal caliceal diverticuli deafness
• Renal carcinoma, familial
• Renal Cell Adenocarcinoma - See Renal cell carcinoma
• Renal cell carcinoma
• Renal cell carcinoma 4
• Renal collecting duct carcinoma - See Collecting duct carcinoma
• Renal coloboma syndrome
• Renal cysts and diabetes syndrome - See Maturity-onset diabetes of the young
• Renal dysplasia diffuse autosomal recessive
• Renal dysplasia diffuse cystic
• Renal dysplasia limb defects syndrome - See Renal dysplasia-limb defects syndrome
• Renal dysplasia or hydronephrosis, oligohydramnios and subsequent lung hypoplasia due to urethral obstruction - SeeUrethral obstruction sequence
• Renal dysplasia retinal aplasia - See Senior Loken Syndrome
• Renal dysplasia, megalocystis, and sirenomelia - See Selig Benacerraf Greene syndrome
• Renal dysplasia, mesomelia, and radiohumeral fusion - See Renal dysplasia-limb defects syndrome
• Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia
• Renal dysplasia-limb defects syndrome
• Renal failure and sensorineural hearing loss - See Autosomal dominant Alport syndrome
• Renal Fanconi syndrome with nephrocalcinosis and renal stones - See Dent disease
• Renal genital middle ear anomalies
• Renal glucosuria - See Renal glycosuria
• Renal glycosuria
• Renal hamartomas, nephroblastomatosis, and fetal gigantism - See Perlman syndrome
• Renal histidinuria - See Histidinuria renal tubular defect
• Renal hypomagnesemia 2
• Renal hypomagnesemia type 2 - See Renal hypomagnesemia 2
• Renal hypomagnesemia-6
• Renal hypouricemia
• Renal medullary carcinoma
• Renal nutcracker syndrome
• Renal oncocytoma
• Renal pelvis and ureter, transitional cell cancer - See Transitional cell cancer of the renal pelvis and ureter
• Renal PHA1 - See Autosomal dominant pseudohypoaldosteronism type 1
• Renal pseudohypoaldosteronism type 1 - See Autosomal dominant pseudohypoaldosteronism type 1
• Renal rickets
• Renal tubular acidosis
• Renal tubular acidosis 1 - See Renal tubular acidosis, distal, autosomal dominant
• Renal tubular acidosis progressive nerve deafness - See Renal tubular acidosis with deafness
• Renal tubular acidosis type 1b - See Renal tubular acidosis with deafness
• Renal tubular acidosis type I - See SLC4A1-associated distal renal tubular acidosis
• Renal tubular acidosis with deafness
• Renal tubular acidosis with progressive nerve deafness - See Renal tubular acidosis with deafness
• Renal tubular acidosis, autosomal recessive with preserved hearing - See Renal tubular acidosis, distal, autosomal recessive
• Renal tubular acidosis, autosomal recessive, with progressive nerve deafness - See Renal tubular acidosis with deafness
• Renal tubular acidosis, distal
• Renal tubular acidosis, distal, autosomal dominant
• Renal tubular acidosis, distal, autosomal recessive
• RENAL TUBULAR ACIDOSIS, DISTAL, AUTOSOMAL RECESSIVE, WITH LATE-ONSET SENSORINEURAL HEARING LOSS, INCLUDED - See Renal tubular acidosis, distal, autosomal recessive
• Renal tubular acidosis, distal, type 3
• Renal tubular acidosis, distal, type 4
• RENAL TUBULAR ACIDOSIS, DISTAL, WITH NORMAL RED CELL MORPHOLOGY, INCLUDED - See Distal renal tubular acidosis with hemolytic anemia
• Renal tubular acidosis, distal, with progressive nerve deafness - See Renal tubular acidosis with deafness
• Renal tubular dysgenesis
• Renal tubulopathy, diabetes mellitus, and cerebellar ataxia due to duplication of mitochondrial DNA
• Renal-ear-anal-radial syndrome - See Townes-Brocks syndrome
• Renal-hepatic-pancreatic dysplasia-Dandy-Walker cysts syndrome - See Dandy-Walker cyst with Renal-Hepatic-Pancreatic dysplasia
• Renal-retinal syndrome - See Senior Loken Syndrome
• REN-associated familial juvenile hyperuricemic nephropathy - See REN-related autosomal dominant tubulointerstitial kidney disease
• REN-associated FJHN - See REN-related autosomal dominant tubulointerstitial kidney disease
• REN-associated kidney disease - See REN-related autosomal dominant tubulointerstitial kidney disease
• REN-associated kidney disease) - See REN-related autosomal dominant tubulointerstitial kidney disease
• Rendu-Osler-Weber disease - See Hereditary hemorrhagic telangiectasia
• Renier Gabreels Jasper syndrome
• Renoanogenital syndrome
• Renoprival hypertension
• Renpenning syndrome 1
• REN-related autosomal dominant tubulointerstitial kidney disease
• RENS1 - See Renpenning syndrome 1
• Resistance to LH (luteinizing hormone)
• Resistance to thyroid stimulating hormone - See Familial hyperthyroidism due to mutations in TSH receptor
• Respiratory distress syndrome, adult - See Acute respiratory distress syndrome
• Respiratory distress syndrome, infant
• Respiratory papillomatosis, recurrent - See Recurrent respiratory papillomatosis
• Restless leg syndrome - See Restless legs syndrome - not a rare disease
• Restless legs syndrome - not a rare disease
• Restless legs syndrome, susceptibility to, 1 - See Restless legs syndrome
• Restless legs syndrome, susceptibility to, 2 - See Restless legs syndrome
• Restless legs syndrome, susceptibility to, 3 - See Restless legs syndrome
• Restless legs syndrome, susceptibility to, 4 - See Restless legs syndrome
• Restless legs syndrome, susceptibility to, 5 - See Restless legs syndrome
• Restless legs syndrome, susceptibility to, 6 - See Restless legs syndrome
• Restrictive dermopathy, lethal - See Tight skin contracture syndrome, lethal
• Retarded growth, hydrocephalus, micrognathia, intestinal malrotation, omphalocele, short lower limbs and foot deformities - See Game Friedman Paradice syndrome
• Retention of dietary cholesterol and abnormal retention of non-cholesterol sterols in the body - See Sitosterolemia
• Reticular dysgenesis
• Reticular pigment anomaly of flexures - See Dowling-Degos disease
• Reticular skin changes, dental anomalies, decreased function of sweat glands, strabismus, and optic atrophy - SeeNaegeli syndrome
• Reticulate acropigmentation of Dohi - See Dyschromatosis symmetrica hereditaria 1
• Reticulate acropigmentation of Kitamura - See Dowling-Degos disease
• Reticulate hyperpigmentation of Iijima - See Linear and whorled nevoid hypermelanosis
• Reticuloendotheliosis
• Reticuloendotheliosis familial with eosinophilia - See Omenn syndrome
• Reticuloendotheliosis, X-linked - See Reticuloendotheliosis
• Reticulohistiocytoma
• Retinal arterial macroaneurysm and supravalvular pulmonic stenosis - See Retinal arterial macroaneurysm with supravalvular pulmonic stenosis
• Retinal arterial macroaneurysm with supravalvular pulmonic stenosis
• Retinal blindness, congenital - See Leber congenital amaurosis
• Retinal cancer - See Retinoblastoma
• Retinal Coloboma - See Retinochoroidal coloboma
• Retinal cone dystrophy 1
• Retinal cone dystrophy 2
• Retinal cone dystrophy 3A
• Retinal cone dystrophy 3B
• Retinal cone dystrophy 4
• Retinal cone-rod dystrophy 2 - See Cone-rod dystrophy 2
• Retinal degeneration with nanophthalmos, cystic macular degeneration, and angle closure glaucoma
• Retinal degeneration, autosomal recessive, prominin-related - See Retinitis pigmentosa
• Retinal degeneration, late-onset, autosomal dominant - See Late-onset retinal degeneration
• Retinal degeneration, nanophthalmos, glaucoma - See Retinal degeneration with nanophthalmos, cystic macular degeneration, and angle closure glaucoma
• Retinal dysplasia X-linked
• Retinal pigment epithelial dystrophy central - See North Carolina macular dystrophy
• Retinal pigmentary degeneration, microcephaly, and severe mental retardation - See Retinopathy pigmentary mental retardation
• Retinal telangiectasia associated with hypogammaglobulinemia - See Frenkel Russe syndrome
• Retinal telangiectasia hypogammaglobulinemia
• Retinal telangiectasis - See Coats disease
• Retinal tumor - See Retinoblastoma
• Retinal vasculopathy and cerebral leukoencephalopathy - See Hereditary endotheliopathy, retinopathy, nephropathy, and stroke
• Retinal vasculopathy and cerebral leukoencephalopathy - See Retinal vasculopathy with cerebral leukodystrophy
• Retinal vasculopathy with cerebral leukodystrophy
• Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations - See Hereditary endotheliopathy, retinopathy, nephropathy, and stroke
• Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations - See Retinal vasculopathy with cerebral leukodystrophy
• Retinis pigmentosa deafness hypogenitalism
• Retinitis pigmentosa
• Retinitis pigmentosa 1 - See Retinitis pigmentosa
• Retinitis Pigmentosa 11 - See Retinitis pigmentosa
• Retinitis pigmentosa 12 - See Retinitis pigmentosa
• Retinitis Pigmentosa 13 - See Retinitis pigmentosa
• Retinitis Pigmentosa 14 - See Retinitis pigmentosa
• Retinitis Pigmentosa 15 - See Retinitis pigmentosa
• Retinitis Pigmentosa 17 - See Retinitis pigmentosa
• Retinitis Pigmentosa 18 - See Retinitis pigmentosa
• Retinitis Pigmentosa 19 - See Retinitis pigmentosa
• Retinitis pigmentosa 2, X-linked - See Retinitis pigmentosa
• Retinitis Pigmentosa 20 - See Retinitis pigmentosa
• Retinitis pigmentosa 21, formerly - See Retinitis pigmentosa-deafness syndrome
• Retinitis Pigmentosa 22 - See Retinitis pigmentosa
• Retinitis Pigmentosa 23 - See Retinitis pigmentosa
• Retinitis Pigmentosa 24 - See Retinitis pigmentosa
• Retinitis Pigmentosa 25 - See Retinitis pigmentosa
• Retinitis Pigmentosa 26 - See Retinitis pigmentosa
• Retinitis Pigmentosa 28 - See Retinitis pigmentosa
• Retinitis pigmentosa 29 - See Retinitis pigmentosa
• Retinitis pigmentosa 3 - See Retinitis pigmentosa
• Retinitis Pigmentosa 30 - See Retinitis pigmentosa
• Retinitis Pigmentosa 31 - See Retinitis pigmentosa
• Retinitis Pigmentosa 32 - See Retinitis pigmentosa
• Retinitis Pigmentosa 33 - See Retinitis pigmentosa
• Retinitis Pigmentosa 34 - See Retinitis pigmentosa
• Retinitis Pigmentosa 35 - See Retinitis pigmentosa
• Retinitis Pigmentosa 36 - See Retinitis pigmentosa
• Retinitis Pigmentosa 4 - See Retinitis pigmentosa
• Retinitis Pigmentosa 41 - See Retinitis pigmentosa
• Retinitis Pigmentosa 6 - See Retinitis pigmentosa
• Retinitis Pigmentosa 7 - See Retinitis pigmentosa