About: Axenfeld-Rieger syndrome     Goto   Sponge   NotDistinct   Permalink

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autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment

AttributesValues
rdf:type
owl:sameAs
description
  • Krankheit (de)
  • sjukdomstillstånd (sv)
  • хвороба (uk)
  • malattia genetica a trasmissione autosomica dominante caratterizzata da anomalie facciali multiple. (it)
  • autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment (en)
exact match
exact match
health specialty
DiseasesDB
Disease Ontology ID
Disease Ontology ID
health specialty
DiseasesDB
  • 30800
Disease Ontology ID
  • DOID:14686
rdfs:label
  • Axenfeld-Rieger syndrome (en)
  • Axenfeld-Riegers syndrom (sv)
  • Rieger-Syndrom (de)
  • Syndroom van Rieger (nl)
  • Síndrome de Axenfeld-Rieger (pt)
  • Zespół Axenfelda-Riegera (pl)
  • axenfeld reider syndroma (hu)
  • axenfeld rieger (es)
  • sindrome di Rieger (it)
  • sindromo de Axenfeld-Rieger (eo)
  • syndrome d'Axenfeld-Rieger (fr)
  • متلازمة أكسينفيلد ريجر (ar)
  • 阿克森費爾德綜合徵 (zh)
skos:prefLabel
  • Axenfeld-Rieger syndrome (en)
  • Axenfeld-Riegers syndrom (sv)
  • Rieger-Syndrom (de)
  • Syndroom van Rieger (nl)
  • Síndrome de Axenfeld-Rieger (pt)
  • Zespół Axenfelda-Riegera (pl)
  • axenfeld reider syndroma (hu)
  • axenfeld rieger (es)
  • sindrome di Rieger (it)
  • sindromo de Axenfeld-Rieger (eo)
  • syndrome d'Axenfeld-Rieger (fr)
  • متلازمة أكسينفيلد ريجر (ar)
  • 阿克森費爾德綜合徵 (zh)
name
  • Axenfeld-Rieger syndrome (en)
  • Axenfeld-Riegers syndrom (sv)
  • Rieger-Syndrom (de)
  • Syndroom van Rieger (nl)
  • Síndrome de Axenfeld-Rieger (pt)
  • Zespół Axenfelda-Riegera (pl)
  • axenfeld reider syndroma (hu)
  • axenfeld rieger (es)
  • sindrome di Rieger (it)
  • sindromo de Axenfeld-Rieger (eo)
  • syndrome d'Axenfeld-Rieger (fr)
  • متلازمة أكسينفيلد ريجر (ar)
  • 阿克森費爾德綜合徵 (zh)
Freebase ID
Freebase ID
  • /m/0gxwc2
instance of
instance of
subclass of
subclass of
KEGG ID
KEGG ID
KEGG ID
  • H00620
Orphanet ID
ICD-10-CM
GARD rare disease ID
Orphanet ID
  • 782
ICD-10-CM
  • Q13.81
GARD rare disease ID
  • 5701
Human Phenotype Ontology ID
Human Phenotype Ontology ID
  • HP:0000558
Commons category
Commons category
  • Axenfeld syndrome
skos:altLabel
  • Anomalia Axenfelda (pl)
  • Anomaly, Rieger's (en)
  • Axenfeld syndrome (en)
  • Axenfeld-Rieger Syndrom (de)
  • Axenfeld-Syndrom (de)
  • Dysgenesis mesodermalis corneae et iridis (de)
  • Hagedoom syndrome (en)
  • Irido-Dentale-Dysplasie (de)
  • RGS - Rieger syndrome (en)
  • Rieger's anomaly (en)
  • Rieger-Axenfeld-Syndrom (de)
  • Zespół Axenfelda (pl)
  • Zespół Axenfelda i Riegera (pl)
  • Zespół Riegera (pl)
NCI Thesaurus ID
Library of Congress authority ID
UMLS CUI
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