MeSH Treeview
Query OMIM entry list
268000
RP
RETINITIS PIGMENTOSA
→
High-scoring List
Neoplasms
Neoplasms by Histologic Type
Neoplasms, Glandular and Epithelial
Adenoma
Growth Hormone-Secreting Pituitary Adenoma
Neoplasms by Site
Breast Neoplasms
Endocrine Gland Neoplasms
Pituitary Neoplasms
Growth Hormone-Secreting Pituitary Adenoma
Neoplastic Processes
Cell Transformation, Neoplastic
Paraneoplastic Syndromes
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Dwarfism, Pituitary
Bone Diseases, Endocrine
Acromegaly
Dwarfism, Pituitary
Hand Deformities
Hand Deformities, Congenital
Joint Diseases
Contracture
Muscular Diseases
Contracture
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Muscular Disorders, Atrophic
Muscular Dystrophies
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Polydactyly
Upper Extremity Deformities, Congenital
Hand Deformities, Congenital
Digestive System Diseases
Gastrointestinal Diseases
Intestinal Diseases
Malabsorption Syndromes
Celiac Disease
Respiratory Tract Diseases
Bronchial Diseases
Bronchiectasis
Kartagener Syndrome
Ciliary Motility Disorders
Kartagener Syndrome
Respiratory System Abnormalities
Kartagener Syndrome
Otorhinolaryngologic Diseases
Ciliary Motility Disorders
Kartagener Syndrome
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Deaf-Blind Disorders
Usher Syndromes
Hearing Loss, Sensorineural
Usher Syndromes
Labyrinth Diseases
Vestibular Diseases
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Huntington Disease
Parkinsonian Disorders
Parkinson Disease
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Peroxisomal Disorders
Mitochondrial Encephalomyopathies
Cerebellar Diseases
Cerebellar Ataxia
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Dementia
Alzheimer Disease
Huntington Disease
Hypothalamic Diseases
Bardet-Biedl Syndrome
Laurence-Moon Syndrome
Pituitary Diseases
Hyperpituitarism
Acromegaly
Hypopituitarism
Dwarfism, Pituitary
Pituitary Neoplasms
Growth Hormone-Secreting Pituitary Adenoma
Movement Disorders
Dyskinesias
Chorea
Huntington Disease
Parkinsonian Disorders
Parkinson Disease
Ocular Motility Disorders
Spinal Cord Diseases
Amyotrophic Lateral Sclerosis
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Cranial Nerve Diseases
Ocular Motility Disorders
Duane Retraction Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Optic Disk Drusen
Papilledema
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Huntington Disease
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
Parkinson Disease
Tauopathies
Alzheimer Disease
TDP-43 Proteinopathies
Amyotrophic Lateral Sclerosis
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Spinocerebellar Ataxias
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Dyslexia
Learning Disorders
Dyslexia
Intellectual Disability
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Deaf-Blind Disorders
Usher Syndromes
Hearing Loss, Sensorineural
Usher Syndromes
Vision Disorders
Blindness
Deaf-Blind Disorders
Usher Syndromes
Color Vision Defects
Hemianopsia
Photophobia
Scotoma
Vision, Low
Neuromuscular Diseases
Motor Neuron Disease
Amyotrophic Lateral Sclerosis
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Sleep Disorders
Dyssomnias
Sleep Disorders, Intrinsic
Disorders of Excessive Somnolence
Eye Diseases
Conjunctival Diseases
Corneal Diseases
Corneal Dystrophies, Hereditary
Eye Abnormalities
Coloboma
Microphthalmos
Retinal Dysplasia
Eye Diseases, Hereditary
Choroideremia
Corneal Dystrophies, Hereditary
Duane Retraction Syndrome
Gyrate Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Retinal Dysplasia
Retinitis Pigmentosa
Eyelid Diseases
Lens Diseases
Cataract
Lens Subluxation
Ocular Hypertension
Glaucoma
Glaucoma, Angle-Closure
Glaucoma, Open-Angle
Ocular Motility Disorders
Duane Retraction Syndrome
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Optic Nerve Diseases
Optic Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Optic Disk Drusen
Papilledema
Refractive Errors
Astigmatism
Hyperopia
Myopia
Retinal Diseases
Diabetic Retinopathy
Retinal Degeneration
Macular Degeneration
Macular Edema
Retinal Dystrophies
Retinitis Pigmentosa
Kearns-Sayre Syndrome
Usher Syndromes
Retinoschisis
Retinal Detachment
Retinal Dysplasia
Retinal Perforations
Uveal Diseases
Choroid Diseases
Choroideremia
Gyrate Atrophy
Iris Diseases
Iridocyclitis
Uveitis
Panuveitis
Uveitis, Anterior
Iridocyclitis
Uveitis, Posterior
Vision Disorders
Blindness
Deaf-Blind Disorders
Usher Syndromes
Hemianopsia
Color Vision Defects
Night Blindness
Photophobia
Scotoma
Vision, Low
Vitreous Detachment
Male Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urologic Diseases
Kidney Diseases
Fanconi Syndrome
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Pregnancy Complications
Fetal Diseases
Prenatal Injuries
Prenatal Exposure Delayed Effects
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Dextrocardia
Kartagener Syndrome
Heart Diseases
Arrhythmias, Cardiac
Bradycardia
Heart Block
Cardiomyopathies
Kearns-Sayre Syndrome
Heart Defects, Congenital
Dextrocardia
Kartagener Syndrome
Myocardial Ischemia
Coronary Disease
Vascular Diseases
Diabetic Angiopathies
Diabetic Retinopathy
Myocardial Ischemia
Coronary Disease
Telangiectasis
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Blood Platelet Disorders
Thrombocytopenia
Hemoglobinopathies
Anemia, Sickle Cell
Leukocyte Disorders
Phagocyte Bactericidal Dysfunction
Granulomatous Disease, Chronic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Bardet-Biedl Syndrome
Deaf-Blind Disorders
Usher Syndromes
Laurence-Moon Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Dextrocardia
Kartagener Syndrome
Chromosome Disorders
Eye Abnormalities
Coloboma
Microphthalmos
Retinal Dysplasia
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Hand Deformities, Congenital
Polydactyly
Respiratory System Abnormalities
Kartagener Syndrome
Situs Inversus
Dextrocardia
Kartagener Syndrome
Fetal Diseases
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Anemia, Sickle Cell
Chromosome Disorders
Dwarfism
Eye Diseases, Hereditary
Choroideremia
Corneal Dystrophies, Hereditary
Duane Retraction Syndrome
Gyrate Atrophy
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Retinal Dysplasia
Retinitis Pigmentosa
Usher Syndromes
Genetic Diseases, X-Linked
Choroideremia
Granulomatous Disease, Chronic
Hemoglobinopathies
Anemia, Sickle Cell
Heredodegenerative Disorders, Nervous System
Huntington Disease
Optic Atrophies, Hereditary
Optic Atrophy, Hereditary, Leber
Spinocerebellar Degenerations
Friedreich Ataxia
Spinocerebellar Ataxias
Kartagener Syndrome
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Peroxisomal Disorders
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Hypobetalipoproteinemias
Peroxisomal Disorders
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Muscular Dystrophies
Skin Diseases, Genetic
Darier Disease
Skin and Connective Tissue Diseases
Skin Diseases
Breast Diseases
Breast Neoplasms
Keratosis
Darier Disease
Skin Diseases, Genetic
Darier Disease
Nutritional and Metabolic Diseases
Metabolic Diseases
Acid-Base Imbalance
Acidosis
Acidosis, Lactic
Ketosis
Diabetic Ketoacidosis
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Peroxisomal Disorders
Mitochondrial Encephalomyopathies
Glucose Metabolism Disorders
Diabetes Mellitus
Diabetes Mellitus, Experimental
Diabetes Mellitus, Type 1
Diabetic Ketoacidosis
Lipid Metabolism Disorders
Dyslipidemias
Hyperlipidemias
Hypolipoproteinemias
Hypobetalipoproteinemias
Malabsorption Syndromes
Celiac Disease
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Peroxisomal Disorders
Lipid Metabolism, Inborn Errors
Hypolipoproteinemias
Hypobetalipoproteinemias
Peroxisomal Disorders
Renal Tubular Transport, Inborn Errors
Fanconi Syndrome
Mitochondrial Diseases
Friedreich Ataxia
Kearns-Sayre Syndrome
Mitochondrial Myopathies
Mitochondrial Encephalomyopathies
Ophthalmoplegia, Chronic Progressive External
Kearns-Sayre Syndrome
Optic Atrophy, Hereditary, Leber
Proteostasis Deficiencies
TDP-43 Proteinopathies
Amyotrophic Lateral Sclerosis
Nutrition Disorders
Malnutrition
Deficiency Diseases
Avitaminosis
Vitamin A Deficiency
Vitamin E Deficiency
Overnutrition
Obesity
Endocrine System Diseases
Diabetes Mellitus
Diabetes Complications
Diabetic Angiopathies
Diabetic Retinopathy
Diabetic Ketoacidosis
Diabetes Mellitus, Experimental
Diabetes Mellitus, Type 1
Dwarfism
Dwarfism, Pituitary
Endocrine Gland Neoplasms
Pituitary Neoplasms
Growth Hormone-Secreting Pituitary Adenoma
Gonadal Disorders
Hypogonadism
Pituitary Diseases
Hyperpituitarism
Acromegaly
Hypopituitarism
Dwarfism, Pituitary
Pituitary Neoplasms
Growth Hormone-Secreting Pituitary Adenoma
Thyroid Diseases
Hypothyroidism
Immune System Diseases
Autoimmune Diseases
Diabetes Mellitus, Type 1
Immunologic Deficiency Syndromes
Phagocyte Bactericidal Dysfunction
Granulomatous Disease, Chronic
Animal Diseases
Cat Diseases
Disease Models, Animal
Dog Diseases
Rodent Diseases
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Atrophy
Pathologic Processes
Arrhythmias, Cardiac
Bradycardia
Heart Block
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Nondisjunction, Genetic
Uniparental Disomy
Sex Chromosome Aberrations
Death
Cadaver
Disease
Syndrome
Disease Attributes
Chronic Disease
Disease Progression
Disease Susceptibility
Genetic Predisposition to Disease
Fibrosis
Gliosis
Neoplastic Processes
Cell Transformation, Neoplastic
Nerve Degeneration
Postoperative Complications
Signs and Symptoms
Body Weight
Overweight
Obesity
Mobility Limitation
Neurologic Manifestations
Dyskinesias
Ataxia
Cerebellar Ataxia
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Dyslexia
Learning Disorders
Dyslexia
Intellectual Disability
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Usher Syndromes
Vision Disorders
Blindness
Color Vision Defects
Hemianopsia
Photophobia
Scotoma
Vision, Low
Sleep Disorders
Signs and Symptoms, Respiratory
Anoxia
Hyperoxia
Wounds and Injuries
Foreign Bodies
Foreign-Body Migration
Radiation Injuries
Radiation Injuries, Experimental
Database Center for Life Science
