About: Adams-Oliver syndrome     Goto   Sponge   NotDistinct   Permalink

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syndrome characterized by defects of the scalp (aplasia cutis congenita), abnormalities of the fingers, toes, arms and legs

AttributesValues
rdf:type
description
  • Krankheit (de)
  • rzadki zespół wad wrodzonych (pl)
  • syndrom (cs)
  • syndrome characterized by defects of the scalp (aplasia cutis congenita), abnormalities of the fingers, toes, arms and legs (en)
  • рідкісний спадковий синдром (uk)
  • raro disturbo congenito con manifestazioni tipiche del cranio e del cuoio capelluto. (it)
exact match
exact match
health specialty
Mondo ID
DiseasesDB
Disease Ontology ID
Mondo ID
Disease Ontology ID
health specialty
Mondo ID
  • MONDO_0007034
DiseasesDB
  • 32741
Disease Ontology ID
  • DOID:0060227
rdfs:label
  • Adams-Oliver syndrome (en)
  • Adams-Oliver sendromu (tr)
  • Adams-Oliver-Syndrom (de)
  • Adams-Oliverův syndrom (cs)
  • Adams–Oliverin oireyhtymä (fi)
  • Zespół Adamsa-Olivera (pl)
  • sindrome di Adams-Oliver (it)
  • syndrome d'Adams-Oliver (fr)
  • синдром Адамса—Олівера (uk)
  • متلازمة آدامز أوليفر (ar)
skos:prefLabel
  • Adams-Oliver syndrome (en)
  • Adams-Oliver sendromu (tr)
  • Adams-Oliver-Syndrom (de)
  • Adams-Oliverův syndrom (cs)
  • Adams–Oliverin oireyhtymä (fi)
  • Zespół Adamsa-Olivera (pl)
  • sindrome di Adams-Oliver (it)
  • syndrome d'Adams-Oliver (fr)
  • синдром Адамса—Олівера (uk)
  • متلازمة آدامز أوليفر (ar)
name
  • Adams-Oliver syndrome (en)
  • Adams-Oliver sendromu (tr)
  • Adams-Oliver-Syndrom (de)
  • Adams-Oliverův syndrom (cs)
  • Adams–Oliverin oireyhtymä (fi)
  • Zespół Adamsa-Olivera (pl)
  • sindrome di Adams-Oliver (it)
  • syndrome d'Adams-Oliver (fr)
  • синдром Адамса—Олівера (uk)
  • متلازمة آدامز أوليفر (ar)
Freebase ID
Freebase ID
  • /m/09w89x
instance of
instance of
subclass of
subclass of
KEGG ID
KEGG ID
KEGG ID
  • H01413
Orphanet ID
ICD-9-CM
genetic association
ICD-10-CM
GARD rare disease ID
OMIM ID
Orphanet ID
  • 974
ICD-9-CM
  • 759.89
genetic association
ICD-10-CM
  • Q87.2
GARD rare disease ID
  • 5739
OMIM ID
  • 100300
  • 614219
  • 616028
  • 615297
  • 614814
named after
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