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ȘTIINȚE APLICATE
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Boli, Tulburări & Simptome
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XX Boli-semne, simptome
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Retinitis Pigmentosa
Informaţii despre
Nume
Retinitis Pigmentosa
Pagina Web
www.malacards.org
Clasificare globală Malacards
Boli genetice
;
Boli rare
Clasificari ICD10
Hereditary retinal dystrophy
Clasificare anatomică Malacards
Boli ale ochiului
Boli din aceeaşi familie
Nonsyndromic Retinitis Pigmentosa
;
Retinitis Pigmentosa 1
;
Retinitis Pigmentosa 10
;
Retinitis Pigmentosa 11
;
Retinitis Pigmentosa 12
;
Retinitis Pigmentosa 13
;
Retinitis Pigmentosa 14
;
Retinitis Pigmentosa 17
;
Retinitis Pigmentosa 18
;
Retinitis Pigmentosa 19
;
Retinitis Pigmentosa 2
;
Retinitis Pigmentosa 20
;
Retinitis Pigmentosa 22
;
Retinitis Pigmentosa 23
;
Retinitis Pigmentosa 24
;
Retinitis Pigmentosa 25
;
Retinitis Pigmentosa 26
;
Retinitis Pigmentosa 27
;
Retinitis Pigmentosa 28
;
Retinitis Pigmentosa 29
;
Retinitis Pigmentosa 3
;
Retinitis Pigmentosa 30
;
Retinitis Pigmentosa 31
;
Retinitis Pigmentosa 32
;
Retinitis Pigmentosa 33
;
Retinitis Pigmentosa 34
;
Retinitis Pigmentosa 35
;
Retinitis Pigmentosa 36
;
Retinitis Pigmentosa 37
;
Retinitis Pigmentosa 38
;
Retinitis Pigmentosa 39
;
Retinitis Pigmentosa 4
;
Retinitis Pigmentosa 40
;
Retinitis Pigmentosa 41
;
Retinitis Pigmentosa 42
;
Retinitis Pigmentosa 43
;
Retinitis Pigmentosa 44
;
Retinitis Pigmentosa 45
;
Retinitis Pigmentosa 46
;
Retinitis Pigmentosa 47
;
Retinitis Pigmentosa 48
;
Retinitis Pigmentosa 49
;
Retinitis Pigmentosa 50
;
Retinitis Pigmentosa 51
;
Retinitis Pigmentosa 54
;
Retinitis Pigmentosa 55
;
Retinitis Pigmentosa 56
;
Retinitis Pigmentosa 57
;
Retinitis Pigmentosa 58
;
Retinitis Pigmentosa 59
;
Retinitis Pigmentosa 6
;
Retinitis Pigmentosa 60
;
Retinitis Pigmentosa 61
;
Retinitis Pigmentosa 62
;
Retinitis Pigmentosa 63
;
Retinitis Pigmentosa 66
;
Retinitis Pigmentosa 67
;
Retinitis Pigmentosa 68
;
Retinitis Pigmentosa 69
;
Retinitis Pigmentosa 7
;
Retinitis Pigmentosa 70
;
Retinitis Pigmentosa 71
;
Retinitis Pigmentosa 72
;
Retinitis Pigmentosa 73
;
Retinitis Pigmentosa 74
;
Retinitis Pigmentosa 75
;
Retinitis Pigmentosa 76
;
Retinitis Pigmentosa 77
;
Retinitis Pigmentosa 78
;
Retinitis Pigmentosa 79
;
Retinitis Pigmentosa 80
;
Retinitis Pigmentosa 81
;
Retinitis Pigmentosa 9
;
Retinitis Pigmentosa, Late-Adult Onset
Vezi şi
Boli A-Z
3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency
Abetalipoproteinemia
Achromatopsia
Achromatopsia 3
Acromegaly
Acute Zonal Occult Outer Retinopathy
Aging
Aland Island Eye Disease
Albinism
Alopecia
Alport Syndrome, X-Linked
Al-Raqad Syndrome
Amyloidosis
Aniridia 1
Aniseikonia
Anorexia Nervosa 1
Arterial Tortuosity Syndrome
Arthritis
Arthrochalasia Ehlers-Danlos Syndrome
Astigmatism
Ataxia and Polyneuropathy, Adult-Onset
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus
Autonomic Dysfunction
Autonomic Neuropathy
Autosomal Dominant Congenital Stationary Night Blindness
Autosomal Dominant Disease
Autosomal Recessive Non-Syndromic Intellectual Disability
Bardet-Biedl Syndrome
Bardet-Biedl Syndrome 1
Bardet-Biedl Syndrome 10
Bardet-Biedl Syndrome 11
Bardet-Biedl Syndrome 12
Bardet-Biedl Syndrome 13
Bardet-Biedl Syndrome 14
Bardet-Biedl Syndrome 15
Bardet-Biedl Syndrome 2
Bardet-Biedl Syndrome 3
Bardet-Biedl Syndrome 4
Bardet-Biedl Syndrome 6
Bardet-Biedl Syndrome 8
Bietti Crystalline Corneoretinal Dystrophy
Bleeding Disorder, Platelet-Type, 11
Blepharophimosis
Blood Group--Ahonen
Blood Group, I System
Blue Cone Monochromacy
Body Dysmorphic Disorder
Body Mass Index Quantitative Trait Locus 10
Body Mass Index Quantitative Trait Locus 11
Body Mass Index Quantitative Trait Locus 12
Body Mass Index Quantitative Trait Locus 14
Body Mass Index Quantitative Trait Locus 18
Body Mass Index Quantitative Trait Locus 4
Body Mass Index Quantitative Trait Locus 7
Body Mass Index Quantitative Trait Locus 8
Body Mass Index Quantitative Trait Locus 9
Brachydactyly
Brachymorphism-Onychodysplasia-Dysphalangism Syndrome
Branch Retinal Artery Occlusion
Bronchiectasis
Cataract
Central Nervous System Disease
Central Retinal Vein Occlusion
Central Serous Chorioretinopathy
Cerebellar Degeneration
Cerebellar Hypoplasia
Ceroid Lipofuscinosis, Neuronal, 3
Cerulean Cataract
Cervicitis
Charles Bonnet Syndrome
Cholestasis
Chorioretinitis
Choroidal Dystrophy, Central Areolar, 1
Choroideremia
Choroiditis
Chronic Granulomatous Disease
Ciliary Dyskinesia, Primary, 1
Ciliopathy
Coats Disease
Color Blindness
Color Vision Deficiency
Common Variable Immunodeficiency
Cone Dystrophy
Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 3
Cone-Rod Dystrophy 6
Cone-Rod Dystrophy 7
Cone-Rod Dystrophy and Hearing Loss
Congenital Hepatic Fibrosis
Congenital Stationary Night Blindness
Congenital Toxoplasmosis
Corneal Dystrophy, Thiel-Behnke Type
Cryptorchidism, Unilateral or Bilateral
Cutis Laxa
Cutis Verticis Gyrata
Cystic Kidney Disease
Deafness, Autosomal Recessive 12
Deafness, Autosomal Recessive 23
Deafness Enamel Hypoplasia Nail Defects
Deafness, X-Linked 2
Degeneration of Macula and Posterior Pole
Dementia
Dextrocardia
Dfnb1
Diabetes Mellitus
Discoid Lupus Erythematosus
Dysautonomia
Enhanced S-Cone Syndrome
Epilepsy
Epithelial Recurrent Erosion Dystrophy
Essential Iris Atrophy
Esterase C
Exfoliation Syndrome
Exotropia
Eye Degenerative Disease
Familial Paroxysmal Nonkinesigenic Dyskinesia
Fanconi Syndrome
Focal Segmental Glomerulosclerosis
Foster-Kennedy Syndrome
Fuchs' Heterochromic Uveitis
Fundus Albipunctatus
Fundus Dystrophy
Glioma
Goldmann-Favre Syndrome
Growth Hormone Deficiency
Gyrate Atrophy of Choroid and Retina
Helix Syndrome
Hematopoietic Stem Cell Transplantation
Hemifacial Atrophy, Progressive
Hemosiderosis
Hepatic Adenomas, Familial
Hepatitis
Hereditary Choroidal Atrophy
Hereditary Night Blindness
Hereditary Retinal Dystrophy
Hydrops, Lactic Acidosis, and Sideroblastic Anemia
Hyperinsulinemic Hypoglycemia
Hyperinsulinemic Hypoglycemia, Familial, 3
Hyperinsulinemic Hypoglycemia, Familial, 4
Hyperinsulinism
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy
Hypoaldosteronism
Hypoglycemia
Hypogonadism
Hypoparathyroidism-Retardation-Dysmorphism Syndrome
Hypophosphatasia
Hypopituitarism
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, and Pallidal Degeneration
Hypoxia
Ichthyosis
Ichthyosis Prematurity Syndrome
Intermediate Uveitis
Interstitial Nephritis
Intrahepatic Cholestasis
Iridocyclitis
Isolated Ectopia Lentis
Joubert Syndrome 1
Keratoconus
Keratomalacia
Late-Onset Retinal Degeneration
Laurence-Moon Syndrome
Leber Congenital Amaurosis
Leber Congenital Amaurosis 1
Leber Congenital Amaurosis 10
Leber Congenital Amaurosis 12
Leber Congenital Amaurosis 14
Leber Congenital Amaurosis 3
Leber Congenital Amaurosis 4
Leber Congenital Amaurosis 5
Leber Congenital Amaurosis 9
Leber Hereditary Optic Neuropathy
Lens Subluxation
Leukemia
Lipid Metabolism Disorder
Lissencephaly
Lupus Erythematosus
Macular Degeneration, Age-Related, 1
Macular Dystrophy, Dominant Cystoid
Macular Dystrophy, Vitelliform, 3
Macular Holes
Macular Retinal Edema
Marfan Syndrome
Mckusick-Kaufman Syndrome
Mcleod Syndrome
Mevalonic Aciduria
Microcephaly
Miller-Dieker Lissencephaly Syndrome
Miyoshi Muscular Dystrophy 1
Mucopolysaccharidosis Iii
Mucopolysaccharidosis-Plus Syndrome
Mucopolysaccharidosis, Type Ii
Mucopolysaccharidosis, Type Iiic
Muscular Dystrophy
Muscular Dystrophy, Duchenne Type
Myopia
Myotonia
Myotonia Atrophica
Myotonic Dystrophy
Nephronophthisis
Nephronophthisis 1
Nephronophthisis 16
Nephronophthisis 2
Nephronophthisis 3
Nervous System Disease
Neurofibromatosis, Type Iv, of Riccardi
Neuronal Ceroid Lipofuscinosis
Neuronitis
Neuropathy
Neuropathy, Ataxia, and Retinitis Pigmentosa
Neuroretinitis
Nevus of Ota
Night Blindness
Night Blindness, Congenital Stationary, Type 2a
Nonsyndromic Retinitis Pigmentosa
Occult Macular Dystrophy
Oliver-Mcfarlane Syndrome
Optic Disk Drusen
Optic Nerve Hypoplasia, Bilateral
Optic Pathway Glioma
Orofaciodigital Syndrome I
Osteochondrodysplasia
Panic Disorder
Papilledema
Paroxysmal Nonkinesigenic Dyskinesia 1
Partial Central Choroid Dystrophy
Peripheral Retinal Degeneration
Peutz-Jeghers Syndrome
Phelan-Mcdermid Syndrome
Phimosis
Pigmented Paravenous Chorioretinal Atrophy
Polycystic Kidney Disease
Polydactyly
Polyneuropathy
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, and Cataract
Posterior Column Ataxia
Posterior Column Ataxia with Retinitis Pigmentosa
Posterior Polar Cataract
Premature Chromatid Separation Trait
Primary Angle-Closure Glaucoma
Primary Ciliary Dyskinesia
Prolonged Electroretinal Response Suppression
Pseudohypoparathyroidism
Pseudoxanthoma Elasticum
Pulmonary Hemosiderosis
Quadriplegia
Radin Blood Group Antigen
Red-Green Color Blindness
Refsum Disease, Classic
Restrictive Dermopathy, Lethal
Reticular Dysgenesis
Retinal Artery Occlusion
Retinal Cone Dystrophy 1
Retinal Degeneration
Retinal Detachment
Retinal Disease
Retinal Vascular Occlusion
Retinal Vein Occlusion
Retinitis
Retinitis Pigmentosa 1
Retinitis Pigmentosa 10
Retinitis Pigmentosa 11
Retinitis Pigmentosa 12
Retinitis Pigmentosa 13
Retinitis Pigmentosa 14
Retinitis Pigmentosa 17
Retinitis Pigmentosa 18
Retinitis Pigmentosa 19
Retinitis Pigmentosa 2
Retinitis Pigmentosa 22
Retinitis Pigmentosa 23
Retinitis Pigmentosa 24
Retinitis Pigmentosa 25
Retinitis Pigmentosa 26
Retinitis Pigmentosa 27
Retinitis Pigmentosa 28
Retinitis Pigmentosa 29
Retinitis Pigmentosa 3
Retinitis Pigmentosa 31
Retinitis Pigmentosa 32
Retinitis Pigmentosa 33
Retinitis Pigmentosa 34
Retinitis Pigmentosa 35
Retinitis Pigmentosa 4
Retinitis Pigmentosa 45
Retinitis Pigmentosa 50
Retinitis Pigmentosa 6
Retinitis Pigmentosa 63
Retinitis Pigmentosa 66
Retinitis Pigmentosa 9
Retinitis Pigmentosa, Y-Linked
Retinopathy, Pericentral Pigmentary, Autosomal Recessive
Retinoschisis 1, X-Linked, Juvenile
Rheumatoid Arthritis
Rhyns Syndrome
Rud Syndrome
Schizophrenia
Scleromalacia Perforans
Seizures, Benign Familial Neonatal, 1
Senior-Løken Syndrome
Senior-Loken Syndrome 1
Sensorineural Hearing Loss
Severe Early-Childhood-Onset Retinal Dystrophy
Sickle Cell Disease
Situs Inversus
Skeletal Dysplasias
Small Cell Carcinoma
Smith-Mccort Dysplasia 1
Spasticity
Spastic Quadriplegia
Spinal and Bulbar Muscular Atrophy, X-Linked 1
Spondylometaphyseal Dysplasia, Axial
Stargardt Disease
Stargardt Disease 1
Stargardt Macular Degeneration
Steatorrhea
Sturge-Weber Syndrome
Tetraamelia Syndrome, Autosomal Recessive
Thalassemia
Thyroiditis
Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations
Toxoplasmoză
Trichomegaly
Trichomegaly with Intellectual Disability, Dwarfism and Pigmentary Degeneration of Retina
Trnt1 Deficiency
Usher Syndrome
Usher Syndrome Type 2
Usher Syndrome, Type I
Usher Syndrome, Type Id
Usher Syndrome, Type if
Usher Syndrome, Type Ig
Usher Syndrome, Type Iia
Usher Syndrome, Type Iic
Usher Syndrome, Type Iid
Usher Syndrome, Type Iiia
Uveitis
Vici Syndrome
Vitelliform Macular Dystrophy
Vitreous Detachment
Weber Syndrome
Weill-Marchesani Syndrome
X-Linked Congenital Stationary Night Blindness
Yemenite Deaf-Blind Hypopigmentation Syndrome
Zimmermann-Laband Syndrome
Zimmermann-Laband Syndrome 1
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