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 Abnormalities

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Hierarchy:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Eye Abnormalities 42 coordinate concepts 8 subordinate concepts ∟ Aniridia \| ∟ Anophthalmos \| ∟ Blepharophimosis \| ∟ Coloboma \| ∟ Ectopia Lentis \| ∟ Hydrophthalmos \| ∟ Microphthalmos \| ∟ Retinal Dysplasia ∟ Abnormalities, Drug-Induced \| ∟ Abnormalities, Multiple \| ∟ Abnormalities, Radiation-Induced \| ∟ Cardiovascular Abnormalities \| ∟ Chromosome Disorders \| ∟ D000013Q000139* \| ∟ DiGeorge Syndrome \| ∟ Digestive System Abnormalities \| ∟ Lymphatic Abnormalities \| ∟ Monsters \| ∟ Musculoskeletal Abnormalities \| ∟ Nervous System Malformations \| ∟ Respiratory System Abnormalities \| ∟ Situs Inversus \| ∟ Skin Abnormalities \| ∟ Stomatognathic System Abnormalities \| ∟ Thyroid Dysgenesis \| ∟ Urogenital Abnormalities \| ∟ Asthenopia \| ∟ Conjunctival Diseases \| ∟ Corneal Diseases \| ∟ Eye Diseases, Hereditary \| ∟ 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 Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Abnormalities 42 coordinate concepts 8 subordinate concepts ∟ Aniridia \| ∟ Anophthalmos \| ∟ Blepharophimosis \| ∟ Coloboma \| ∟ Ectopia Lentis \| ∟ Hydrophthalmos \| ∟ Microphthalmos \| ∟ Retinal Dysplasia ∟ Abnormalities, Drug-Induced \| ∟ Abnormalities, Multiple \| ∟ Abnormalities, Radiation-Induced \| ∟ Cardiovascular Abnormalities \| ∟ Chromosome Disorders \| ∟ D000013Q000139* \| ∟ DiGeorge Syndrome \| ∟ Digestive System Abnormalities \| ∟ Lymphatic Abnormalities \| ∟ Monsters \| ∟ Musculoskeletal Abnormalities \| ∟ Nervous System Malformations \| ∟ Respiratory System Abnormalities \| ∟ Situs Inversus \| ∟ Skin Abnormalities \| ∟ Stomatognathic System Abnormalities \| ∟ Thyroid Dysgenesis \| ∟ Urogenital Abnormalities \| ∟ Asthenopia \| ∟ Conjunctival Diseases \| ∟ Corneal Diseases \| ∟ Eye Diseases, Hereditary \| ∟ 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 X
Broader terms:	Medical Subject Headings (MeSH) ∟ Congenital, Hereditary, and Neonatal Diseases and Abnormalities ∟ Abnormalities ∟ Eye Abnormalities Medical Subject Headings (MeSH) ∟ Eye Diseases ∟ Eye Abnormalities Abnormalities > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Medical Subject Headings (MeSH) Eye Diseases > Medical Subject Headings (MeSH) X
Narrower terms:	Aniridia \| Anophthalmos \| Blepharophimosis \| Coloboma \| Ectopia Lentis \| Hydrophthalmos \| Microphthalmos \| Retinal Dysplasia X
Annotation:	do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; these are structural abnorm: EYE DISEASES, HEREDITARY is also available X
History note:	Eye/abnormalities (1977-1989) \| specific eye heading/abnormalities (1977-1989)X
historyNote*:	90; was NON MESH 1977-89 X
publicMeSHNote*:	90 X
Scope note:	Congenital absence of or defects in structures of the eye; may also be hereditary. X
activeMeSHYear*:	2000 \| 2001 \| 2002 \| 2003 \| 2004 \| 2005 \| 2006 \| 2007X
dateCreated*:	1999-01-01X
dateEstablished*:	1990-01-01X
dateRevised*:	1999-11-03X
recordAuthorizer*:	sjnX
recordMaintainer*:	kleX
recordOriginator*:	NLMX
Type:	Concept X
Coordinate terms:	Abnormalities, Drug-Induced \| Abnormalities, Multiple \| Abnormalities, Radiation-Induced \| Cardiovascular Abnormalities \| Chromosome Disorders \| D000013Q000139* \| DiGeorge Syndrome \| Digestive System Abnormalities \| Lymphatic Abnormalities \| Monsters \| Musculoskeletal Abnormalities \| Nervous System Malformations \| Respiratory System Abnormalities \| Situs Inversus \| Skin Abnormalities \| Stomatognathic System Abnormalities \| Thyroid Dysgenesis \| Urogenital Abnormalities \| Asthenopia \| Conjunctival Diseases \| Corneal Diseases \| Eye Diseases, Hereditary \| 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 X
URI:	X
Labels and equivalent concepts:	Silmien epämuodostumat (fi) Silmien kehityshäiriöt (fi, replaced) Silmien poikkeamat (fi, replaced) Silmän poikkeama (fi, replaced) Silmän kehityshäiriö (fi, replaced) Poikkevat silmät (fi, replaced) Silmän epämuodostuma (fi, replaced) Poikkeva silmä (fi, replaced) Ögonmissbildningar (sv) X
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