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Human disease

AttributesValues
rdf:type
description
  • Krankheit (de)
  • Human disease (en)
  • մարդու հիվանդություն (hy)
  • хвороба людини (uk)
  • مرض يصيب الإنسان (ar)
  • malattia ereditaria (it)
  • trastorn autosòmic recessiu (ca)
exact match
exact match
health specialty
ICD-10
Mondo ID
DiseasesDB
Disease Ontology ID
symptoms and signs
Mondo ID
Disease Ontology ID
health specialty
ICD-10
  • Q87.1
Mondo ID
  • MONDO_0009955
DiseasesDB
  • 34465
Disease Ontology ID
  • DOID:0050774
symptoms and signs
rdfs:label
  • Hội chứng RAPADILINO (vi)
  • RAPADILINO sendromu (tr)
  • RAPADILINO-Syndrom (de)
  • RAPADILINO-oireyhtymä (fi)
  • Sindrome Rapadilino (it)
  • Síndrome RAPADILINO (ca)
  • Zespół RAPADILINO (pl)
  • rapadilino syndrome (en)
  • syndrome Rapadilano (fr)
  • متلازمة راباديلينو (ar)
skos:prefLabel
  • Hội chứng RAPADILINO (vi)
  • RAPADILINO sendromu (tr)
  • RAPADILINO-Syndrom (de)
  • RAPADILINO-oireyhtymä (fi)
  • Sindrome Rapadilino (it)
  • Síndrome RAPADILINO (ca)
  • Zespół RAPADILINO (pl)
  • rapadilino syndrome (en)
  • syndrome Rapadilano (fr)
  • متلازمة راباديلينو (ar)
name
  • Hội chứng RAPADILINO (vi)
  • RAPADILINO sendromu (tr)
  • RAPADILINO-Syndrom (de)
  • RAPADILINO-oireyhtymä (fi)
  • Sindrome Rapadilino (it)
  • Síndrome RAPADILINO (ca)
  • Zespół RAPADILINO (pl)
  • rapadilino syndrome (en)
  • syndrome Rapadilano (fr)
  • متلازمة راباديلينو (ar)
Freebase ID
Freebase ID
  • /m/026rmlw
instance of
instance of
subclass of
subclass of
KEGG ID
KEGG ID
KEGG ID
  • H00965
UniProt disease ID
Orphanet ID
ICD-9-CM
genetic association
ICD-10-CM
GARD rare disease ID
OMIM ID
Genetics Home Reference Conditions ID
UniProt disease ID
  • DI-02245
Orphanet ID
  • 3021
ICD-9-CM
  • 759.89
genetic association
ICD-10-CM
  • Q87.1
GARD rare disease ID
  • 4637
OMIM ID
  • 266280
Genetics Home Reference Conditions ID
  • rapadilino-syndrome
skos:altLabel
  • RAPADILINO SYNDROME (en)
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