About: Usher syndrome type 1K     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

An Usher syndrome type 1 that has material basis in variation in the chromosome region 10p11.21-q21.1.

AttributesValues
rdf:type
description
  • An Usher syndrome type 1 that has material basis in variation in the chromosome region 10p11.21-q21.1. (en)
exact match
exact match
Mondo ID
Disease Ontology ID
Mondo ID
Disease Ontology ID
Mondo ID
  • MONDO_0014001
Disease Ontology ID
  • DOID:0110837
rdfs:label
  • Usher syndrome type 1K (en)
skos:prefLabel
  • Usher syndrome type 1K (en)
name
  • Usher syndrome type 1K (en)
instance of
instance of
subclass of
subclass of
ICD-10-CM
OMIM ID
ICD-10-CM
  • H35.5
OMIM ID
  • 614990
skos:altLabel
  • USH1K (en)
  • USHER SYNDROME, TYPE IK (en)
  • USHER SYNDROME, TYPE IK; USH1K (en)
  • Usher syndrome type IK (en)
UMLS CUI
on focus list of Wikimedia project
UMLS CUI
  • C3539124
on focus list of Wikimedia project
is about of
Faceted Search & Find service v1.16.117 as of May 05 2024


Alternative Linked Data Documents: ODE     Content Formats:   [cxml] [csv]     RDF   [text] [turtle] [ld+json] [rdf+json] [rdf+xml]     ODATA   [atom+xml] [odata+json]     Microdata   [microdata+json] [html]    About   
This material is Open Knowledge   W3C Semantic Web Technology [RDF Data] Valid XHTML + RDFa
OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 172 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software