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human disease

AttributesValues
rdf:type
owl:sameAs
description
  • human disease (en)
  • մարդու հիվանդություն (hy)
  • хвороба людини (uk)
exact match
exact match
Mondo ID
Disease Ontology ID
Mondo ID
Disease Ontology ID
Mondo ID
  • MONDO_0009903
Disease Ontology ID
  • DOID:0111259
rdfs:label
  • Sindrome di Miller (it)
  • Miller syndrome (en)
  • Syndroom van Miller (nl)
  • dysostose acrofaciale postaxiale (fr)
skos:prefLabel
  • Sindrome di Miller (it)
  • Miller syndrome (en)
  • Syndroom van Miller (nl)
  • dysostose acrofaciale postaxiale (fr)
name
  • Sindrome di Miller (it)
  • Miller syndrome (en)
  • Syndroom van Miller (nl)
  • dysostose acrofaciale postaxiale (fr)
instance of
instance of
subclass of
subclass of
UniProt disease ID
Orphanet ID
ICD-9-CM
genetic association
ICD-10-CM
PatientsLikeMe condition ID
GARD rare disease ID
OMIM ID
Genetics Home Reference Conditions ID
UniProt disease ID
  • DI-02571
Orphanet ID
  • 246
ICD-9-CM
  • 759.89
genetic association
ICD-10-CM
  • Q75.4
PatientsLikeMe condition ID
  • miller-syndrome
GARD rare disease ID
  • 8410
OMIM ID
  • 263750
Genetics Home Reference Conditions ID
  • miller-syndrome
skos:altLabel
  • Acrofacial dysostosis, Genee-Wiedmann type (en)
  • Genee-Wiedemann Syndrome (en)
  • Miller Syndrome (en)
  • POADS (en)
  • POSTAXIAL ACROFACIAL DYSOSTOSIS (en)
  • POSTAXIAL ACROFACIAL DYSOSTOSIS; POADS (en)
  • Postaxial acrodysostosis (en)
  • acrofacial dysostosis, Genee-Wiedmann type (en)
  • postaxial acrofacial dysostosis (en)
  • mandibulfacial dysostosis with postaxial limb anomalies (en)
  • Mandibulfacial dysostosis with postaxial limb anomalies (en)
WikiKids ID
UMLS CUI
MeSH descriptor ID
on focus list of Wikimedia project
Microsoft Academic ID
ICD-11 (foundation)
MeSH descriptor ID
Microsoft Academic ID
WikiKids ID
  • Syndroom_van_Miller
UMLS CUI
  • C0265257
MeSH descriptor ID
  • C537680
on focus list of Wikimedia project
Microsoft Academic ID
  • 2778320226
ICD-11 (foundation)
  • 70602060
WikiProjectMed ID
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