ONKI3 | Medical Subject Headings

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The way property values are displayed: value/row values side by side

The way concept relations are shown: separately in hierarchy

Eye Diseases, Hereditary

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary 58 coordinate concepts 10 subordinate concepts ∟ Albinism \| ∟ Aniridia \| ∟ Choroideremia \| ∟ Corneal Dystrophies, Hereditary \| ∟ Duane Retraction Syndrome \| ∟ Graves Ophthalmopathy \| ∟ Gyrate Atrophy \| ∟ Optic Atrophies, Hereditary \| ∟ Retinal Dysplasia \| ∟ Retinitis Pigmentosa ∟ Asthenopia \| ∟ Conjunctival Diseases \| ∟ Corneal Diseases \| ∟ Eye Abnormalities \| ∟ Eye Hemorrhage \| ∟ Eye Infections \| ∟ Eye Manifestations \| ∟ Eye Neoplasms \| ∟ Eyelid Diseases \| ∟ Lacrimal Apparatus Diseases \| ∟ Lens Diseases \| ∟ Ocular Hypertension \| ∟ Ocular Hypotension \| ∟ Ocular Motility Disorders \| ∟ Optic Nerve Diseases \| ∟ Orbital Diseases \| ∟ Pupil Disorders \| ∟ Refractive Errors \| ∟ Retinal Diseases \| ∟ Scleral Diseases \| ∟ Uveal Diseases \| ∟ Vision Disorders \| ∟ Vitreoretinopathy, Proliferative \| ∟ Vitreous Detachment \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary 58 coordinate concepts 10 subordinate concepts ∟ Albinism \| ∟ Aniridia \| ∟ Choroideremia \| ∟ Corneal Dystrophies, Hereditary \| ∟ Duane Retraction Syndrome \| ∟ Graves Ophthalmopathy \| ∟ Gyrate Atrophy \| ∟ Optic Atrophies, Hereditary \| ∟ Retinal Dysplasia \| ∟ Retinitis Pigmentosa ∟ Asthenopia \| ∟ Conjunctival Diseases \| ∟ Corneal Diseases \| ∟ Eye Abnormalities \| ∟ Eye Hemorrhage \| ∟ Eye Infections \| ∟ Eye Manifestations \| ∟ Eye Neoplasms \| ∟ Eyelid Diseases \| ∟ Lacrimal Apparatus Diseases \| ∟ Lens Diseases \| ∟ Ocular Hypertension \| ∟ Ocular Hypotension \| ∟ Ocular Motility Disorders \| ∟ Optic Nerve Diseases \| ∟ Orbital Diseases \| ∟ Pupil Disorders \| ∟ Refractive Errors \| ∟ Retinal Diseases \| ∟ Scleral Diseases \| ∟ Uveal Diseases \| ∟ Vision Disorders \| ∟ Vitreoretinopathy, Proliferative \| ∟ Vitreous Detachment \| ∟ Adrenal Hyperplasia, Congenital \| ∟ Anemia, Hemolytic, Congenital \| ∟ Anemia, Hypoplastic, Congenital \| ∟ Ataxia Telangiectasia \| ∟ Blood Coagulation Disorders, Inherited \| ∟ Brugada Syndrome \| ∟ CADASIL \| ∟ Camurati-Engelmann Syndrome \| ∟ Cardiomyopathy, Hypertrophic, Familial \| ∟ Cherubism \| ∟ Chromosome Disorders \| ∟ Cystic Fibrosis \| ∟ Dwarfism \| ∟ Familial Mediterranean Fever \| ∟ Genetic Diseases, X-Linked \| ∟ Genetic Diseases, Y-Linked \| ∟ Hajdu-Cheney Syndrome \| ∟ Hemoglobinopathies \| ∟ Heredodegenerative Disorders, Nervous System \| ∟ Hyperthyroxinemia, Familial Dysalbuminemic \| ∟ Jervell-Lange Nielsen Syndrome \| ∟ Kallmann Syndrome \| ∟ Kartagener Syndrome \| ∟ Marfan Syndrome \| ∟ Metabolism, Inborn Errors \| ∟ Muscular Dystrophies \| ∟ Myasthenic Syndromes, Congenital \| ∟ Nail-Patella Syndrome \| ∟ Neoplastic Syndromes, Hereditary \| ∟ Osteogenesis Imperfecta \| ∟ Pain Insensitivity, Congenital \| ∟ Romano-Ward Syndrome \| ∟ Skin Diseases, Genetic \| ∟ Werner Syndrome X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Genetic Diseases, Inborn ∟ Eye Diseases, Hereditary Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Diseases, Hereditary Genetic Diseases, Inborn > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Eye Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Albinism \| Aniridia \| Choroideremia \| Corneal Dystrophies, Hereditary \| Duane Retraction Syndrome \| Graves Ophthalmopathy \| Gyrate Atrophy \| Optic Atrophies, Hereditary \| Retinal Dysplasia \| Retinitis Pigmentosa X
History note:	Eye Diseases/genetics (1966-1989)X
historyNote*:	90 X
publicMeSHNote*:	90 X
Scope note:	Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder. X
activeMeSHYear*:	2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1989-09-06X
dateEstablished*:	1990-01-01X
dateRevised*:	2001-07-25X
recordAuthorizer*:	sjnX
recordMaintainer*:	nnsX
recordOriginator*:	EGCX
Type:	Concept X
Coordinate terms:	Asthenopia \| Conjunctival Diseases \| Corneal Diseases \| Eye Abnormalities \| Eye Hemorrhage \| Eye Infections \| Eye Manifestations \| Eye Neoplasms \| Eyelid Diseases \| Lacrimal Apparatus Diseases \| Lens Diseases \| Ocular Hypertension \| Ocular Hypotension \| Ocular Motility Disorders \| Optic Nerve Diseases \| Orbital Diseases \| Pupil Disorders \| Refractive Errors \| Retinal Diseases \| Scleral Diseases \| Uveal Diseases \| Vision Disorders \| Vitreoretinopathy, Proliferative \| Vitreous Detachment \| Adrenal Hyperplasia, Congenital \| Anemia, Hemolytic, Congenital \| Anemia, Hypoplastic, Congenital \| Ataxia Telangiectasia \| Blood Coagulation Disorders, Inherited \| Brugada Syndrome \| CADASIL \| Camurati-Engelmann Syndrome \| Cardiomyopathy, Hypertrophic, Familial \| Cherubism \| Chromosome Disorders \| Cystic Fibrosis \| Dwarfism \| Familial Mediterranean Fever \| Genetic Diseases, X-Linked \| Genetic Diseases, Y-Linked \| Hajdu-Cheney Syndrome \| Hemoglobinopathies \| Heredodegenerative Disorders, Nervous System \| Hyperthyroxinemia, Familial Dysalbuminemic \| Jervell-Lange Nielsen Syndrome \| Kallmann Syndrome \| Kartagener Syndrome \| Marfan Syndrome \| Metabolism, Inborn Errors \| Muscular Dystrophies \| Myasthenic Syndromes, Congenital \| Nail-Patella Syndrome \| Neoplastic Syndromes, Hereditary \| Osteogenesis Imperfecta \| Pain Insensitivity, Congenital \| Romano-Ward Syndrome \| Skin Diseases, Genetic \| Werner Syndrome X
URI:	X
Labels and equivalent concepts:	Perinnölliset silmätaudit (fi) Periytyvät silmätaudit (fi, replaced) Periytyvät silmäsairaudet (fi, replaced) Perinnölliset silmäsairaudet (fi, replaced) Hereditaariset silmäsairaudet (fi, replaced) Hereditaariset silmätaudit (fi, replaced) Ögonsjukdomar, ärftliga (sv) Ärftliga ögonsjukdomar (sv, replaced) Hereditary Eye Diseases (en, replaced) X
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