Visual impairment - Ontology Report - Rat Genome Database

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HUMAN PHENOTYPE - ANNOTATIONS	{{ watchLinkText }}
The Human Phenotype Ontology (HPO) is downloaded weekly from http://compbio.charite.de/hudson/job/hpo/lastStableBuild/artifact/ontology/release/hp.obo. The file downloaded is considered the "last stable build" available for the ontology. For more about the HPO, view their website at http://www.human-phenotype-ontology.org/.

Term:	Visual impairment	go back to main search page
Accession:	HP:0000505	browse the term
Definition:	Visual impairment (or vision impairment) is vision loss (of a person) to such a degree as to qualify as an additional support need through a significant limitation of visual capability resulting from either disease, trauma, or congenital or degenerative conditions that cannot be corrected by conventional means, such as refractive correction, medication, or surgery.
Synonyms:	exact_synonym:	Impaired vision; Loss of eyesight; Poor vision
	alt_id:	HP:0000516; HP:0000566; HP:0007758; HP:0007860; HP:0007983
	xref:	MESH:D014786; MESH:D015354; SNOMEDCT_US:246635007; SNOMEDCT_US:397540003; SNOMEDCT_US:7973008; UMLS:C0042798; UMLS:C3665347

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Term paths to the root

Path 1
Term	Annotations
Human phenotype	0
Phenotypic abnormality	0
Abnormality of the eye	0
Abnormal eye physiology	0
Abnormality of vision	0
Visual impairment	0
Cerebral visual impairment	0
Reduced visual acuity +	0
Visual field defect +	0
Visual loss +	0

paths to the root