Not logged in : Login
(Sponging disallowed)

About: amelogenesis imperfecta hypomaturation type 2A3     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

AttributesValues
type
subClassOf
label
  • amelogenesis imperfecta hypomaturation type 2A3
described by
id
  • DOID:0110061
database_cross_reference
  • ICD10CM:K00.5
  • OMIM:613211
has_exact_synonym
  • AI2A3 (en)
  • amelogenesis imperfecta hypomaturation type IIA3 (en)
  • amelogenesis imperfecta type IIA3 (en)
has_obo_namespace
  • disease_ontology
http://purl.obolib...g/obo/IAO_0000115
  • An amelogenesis imperfecta caused by homozygous mutation in the WDR72 gene.
is topic of
is annotatedSource of
Faceted Search & Find service v1.17_git149 as of Dec 03 2024


Alternative Linked Data Documents: iSPARQL | 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 08.03.3332 as of Jan 29 2025, on Linux (x86_64-generic-linux-glibc25), Single-Server Edition (378 GB total memory, 14 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software