About: hypertrophic cardiomyopathy 16     Goto   Sponge   NotDistinct   Permalink

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hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYOZ2 gene on chromosome 4q26

AttributesValues
rdf:type
description
  • Krankheit (de)
  • مرض يصيب الإنسان (ar)
  • хвороба (uk)
  • hypertrophic cardiomyopathy that has material basis in heterozygous mutation in the MYOZ2 gene on chromosome 4q26 (en)
exact match
exact match
Mondo ID
Disease Ontology ID
Mondo ID
Disease Ontology ID
Mondo ID
  • MONDO_0013455
Disease Ontology ID
  • DOID:0110322
rdfs:label
  • hypertrophic cardiomyopathy 16 (en)
skos:prefLabel
  • hypertrophic cardiomyopathy 16 (en)
name
  • hypertrophic cardiomyopathy 16 (en)
instance of
instance of
subclass of
subclass of
UniProt disease ID
Orphanet ID
genetic association
OMIM ID
UniProt disease ID
  • DI-03037
Orphanet ID
  • 155
genetic association
OMIM ID
  • 613838
skos:altLabel
  • CMH16 (en)
  • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16 (en)
  • CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; CMH16 (en)
  • Cardiomyopathy, Familial Hypertrophic, type 16 (en)
  • cardiomyopathy familial hypertrophic 16 (en)
  • hypertrophic cardiomyopathy type 16 (en)
UMLS CUI
on focus list of Wikimedia project
UMLS CUI
  • C3151204
on focus list of Wikimedia project
is about of
is genetic association of
is genetic association of
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