This HTML5 document contains 18 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
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n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
n5	http://purl.obolibrary.org/obo/doid#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

n2:DOID_13911

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_13399

rdfs:label

achromatopsia

wdrs:describedby

n8:doid.owl

obo:id

DOID:13911

obo:hasDbXref

UMLS_CUI:C0152200 NCI:C84528 ICD9CM:368.54 SNOMEDCT_US_2021_09_01:56852002 ICD10CM:H53.51 ORDO:49382 MESH:D003117

obo:hasExactSynonym

ACHM Monochromatism

obo:hasOBONamespace

disease_ontology

obo:inSubset

n5:DO_rare_slim n5:NCIthesaurus

n2:IAO_0000115

A color blindness that is characterized by a congenital cone color vision disorder, the inability to perceive color and to achieve satisfactory visual acuity at high light levels has_material_basis_in autosomal recessive inheritance.