About: Bannayan-Riley-Ruvalcaba syndrome     Goto   Sponge   NotDistinct   Permalink

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a rare overgrowth syndrome and hamartomatous disorder with occurrence of multiple subcutaneous lipomas, macrocephaly and hemangiomas.

AttributesValues
rdf:type
owl:sameAs
description
  • Krankheit (de)
  • مرض يصيب الإنسان (ar)
  • хвороба (uk)
  • malattia genetica rara (it)
  • a rare overgrowth syndrome and hamartomatous disorder with occurrence of multiple subcutaneous lipomas, macrocephaly and hemangiomas. (en)
exact match
exact match
health specialty
Mondo ID
DiseasesDB
Disease Ontology ID
Mondo ID
Disease Ontology ID
health specialty
Mondo ID
  • MONDO_0007924
DiseasesDB
  • 31337
Disease Ontology ID
  • DOID:0050657
rdfs:label
  • Bannayan-Riley-Ruvalcaba syndrome (en)
  • Bannayan-Riley-Ruvalcaba sendromu (tr)
  • Ruvalcaba-Myhre-Smith-Syndrom (de)
  • Sindrome di Bannayan-Riley-Ruvalcaba (it)
  • Síndrome de Bannayan–Riley–Ruvalcaba (ca)
  • Zespół Bannayana-Rileya-Ruvalcaby (pl)
  • syndrome de Bannayan-Riley-Ruvalcaba (fr)
  • متلازمة بانيان- رايلي- روفالكابا (ar)
  • バナヤン・ライリー・ルバルカバ症候群 (ja)
skos:prefLabel
  • Bannayan-Riley-Ruvalcaba syndrome (en)
  • Bannayan-Riley-Ruvalcaba sendromu (tr)
  • Ruvalcaba-Myhre-Smith-Syndrom (de)
  • Sindrome di Bannayan-Riley-Ruvalcaba (it)
  • Síndrome de Bannayan–Riley–Ruvalcaba (ca)
  • Zespół Bannayana-Rileya-Ruvalcaby (pl)
  • syndrome de Bannayan-Riley-Ruvalcaba (fr)
  • متلازمة بانيان- رايلي- روفالكابا (ar)
  • バナヤン・ライリー・ルバルカバ症候群 (ja)
name
  • Bannayan-Riley-Ruvalcaba syndrome (en)
  • Bannayan-Riley-Ruvalcaba sendromu (tr)
  • Ruvalcaba-Myhre-Smith-Syndrom (de)
  • Sindrome di Bannayan-Riley-Ruvalcaba (it)
  • Síndrome de Bannayan–Riley–Ruvalcaba (ca)
  • Zespół Bannayana-Rileya-Ruvalcaby (pl)
  • syndrome de Bannayan-Riley-Ruvalcaba (fr)
  • متلازمة بانيان- رايلي- روفالكابا (ar)
  • バナヤン・ライリー・ルバルカバ症候群 (ja)
Freebase ID
Freebase ID
  • /m/0bdch8
instance of
instance of
subclass of
subclass of
Orphanet ID
ICD-9-CM
genetic association
ICD-10-CM
PatientsLikeMe condition ID
GARD rare disease ID
OMIM ID
Orphanet ID
  • 109
ICD-9-CM
  • 759.6
genetic association
ICD-10-CM
  • Q87.8
  • Q87.89
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