This HTML5 document contains 17 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

Namespace Prefixes

Prefix	IRI
n6	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
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#
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_0110031

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_1099

rdfs:label

hemoglobin H disease

wdrs:describedby

n6:doid.owl

obo:id

DOID:0110031

obo:hasDbXref

OMIM:613978 ORDO:93616 ICD10CM:D56.0

obo:hasExactSynonym

alpha thalassemia, haemoglobin H type alpha thalassemia, hemoglobin H type hemoglobin H disease, deletional alpha-thalassemia intermedia HBH haemoglobin H disease haemoglobin H disease, deletional

obo:hasOBONamespace

disease_ontology

n2:IAO_0000115

An alpha thalassemia that has_material_basis_in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other.