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genetic disorder inherited in an autosomal dominant manner that is characterized by early, and frequently severe, high blood pressure

AttributesValues
rdf:type
description
  • Krankheit (de)
  • مرض يصيب الإنسان (ar)
  • хвороба (uk)
  • malaltia minoritària (ca)
  • forma di pseudoaldosteronismo che compare in giovane etá (it)
  • genetic disorder inherited in an autosomal dominant manner that is characterized by early, and frequently severe, high blood pressure (en)
  • choroba genetyczna u ludzi (pl)
exact match
exact match
health specialty
ICD-10
Mondo ID
DiseasesDB
Disease Ontology ID
Mondo ID
Disease Ontology ID
health specialty
ICD-10
  • I15.1
Mondo ID
  • MONDO_0008323
DiseasesDB
  • 7471
Disease Ontology ID
  • DOID:0050477
rdfs:label
  • Hội chứng Liddle (vi)
  • Liddle syndrome (en)
  • Liddle-Syndrom (de)
  • Liddlen oireyhtymä (fi)
  • Liddleov sindrom (bs)
  • Liddleov sindrom (hr)
  • Síndrome de Liddle (ca)
  • Síndrome de Liddle (es)
  • Síndrome de Liddle (pt)
  • Zespół Liddle'a (pl)
  • sindrome di Liddle (it)
  • sindromo de Liddle (eo)
  • syndrome de Liddle (fr)
  • Синдром Лиддла (ru)
  • متلازمة ليدل (ar)
  • リドル症候群 (ja)
  • 李德爾氏綜合徵 (zh)
skos:prefLabel
  • Hội chứng Liddle (vi)
  • Liddle syndrome (en)
  • Liddle-Syndrom (de)
  • Liddlen oireyhtymä (fi)
  • Liddleov sindrom (bs)
  • Liddleov sindrom (hr)
  • Síndrome de Liddle (ca)
  • Síndrome de Liddle (es)
  • Síndrome de Liddle (pt)
  • Zespół Liddle'a (pl)
  • sindrome di Liddle (it)
  • sindromo de Liddle (eo)
  • syndrome de Liddle (fr)
  • Синдром Лиддла (ru)
  • متلازمة ليدل (ar)
  • リドル症候群 (ja)
  • 李德爾氏綜合徵 (zh)
name
  • Hội chứng Liddle (vi)
  • Liddle syndrome (en)
  • Liddle-Syndrom (de)
  • Liddlen oireyhtymä (fi)
  • Liddleov sindrom (bs)
  • Liddleov sindrom (hr)
  • Síndrome de Liddle (ca)
  • Síndrome de Liddle (es)
  • Síndrome de Liddle (pt)
  • Zespół Liddle'a (pl)
  • sindrome di Liddle (it)
  • sindromo de Liddle (eo)
  • syndrome de Liddle (fr)
  • Синдром Лиддла (ru)
  • متلازمة ليدل (ar)
  • リドル症候群 (ja)
  • 李德爾氏綜合徵 (zh)
Freebase ID
Freebase ID
  • /m/0bdbsd
instance of
instance of
subclass of
subclass of
KEGG ID
KEGG ID
KEGG ID
  • H00242
UniProt disease ID
Orphanet ID
genetic association
ICD-10-CM
PatientsLikeMe condition ID
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