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- Aase_syndrome abstract "Aase syndrome or Aase–Smith syndrome is a rare inherited disorder characterized by anemia with some joint and skeletal deformities. Aase syndrome is thought to be an autosomal recessive inherited disorder. The genetic basis of the disease is not known. The anemia is caused by underdevelopment of the bone marrow, which is where blood cells are formed.It is named after the American paediatricians Jon Morton Aase and David Weyhe Smith, who characterized it in 1968.".
- Aase_syndrome diseasesdb "29332".
- Aase_syndrome medlineplus "001662".
- Aase_syndrome omim "147800".
- Aase_syndrome wikiPageID "1126118".
- Aase_syndrome wikiPageRevisionID "560019878".
- Aase_syndrome diseasesdb "29332".
- Aase_syndrome hasPhotoCollection Aase_syndrome.
- Aase_syndrome medlineplus "1662".
- Aase_syndrome name "Aase syndrome".
- Aase_syndrome omim "147800".
- Aase_syndrome wordnet_type synset-disease-noun-1.
- Aase_syndrome subject Category:Genetic_disorders_with_OMIM_but_no_gene.
- Aase_syndrome subject Category:Syndromes.
- Aase_syndrome type Abstraction100002137.
- Aase_syndrome type Attribute100024264.
- Aase_syndrome type Cognition100023271.
- Aase_syndrome type Complex105870365.
- Aase_syndrome type Concept105835747.
- Aase_syndrome type Condition113920835.
- Aase_syndrome type Content105809192.
- Aase_syndrome type Disease114070360.
- Aase_syndrome type GeneticDisease114151139.
- Aase_syndrome type GeneticDisordersWithOMIMButNoGene.
- Aase_syndrome type Idea105833840.
- Aase_syndrome type IllHealth114052046.
- Aase_syndrome type Illness114061805.
- Aase_syndrome type PathologicalState114051917.
- Aase_syndrome type PhysicalCondition114034177.
- Aase_syndrome type PsychologicalFeature100023100.
- Aase_syndrome type State100024720.
- Aase_syndrome type Syndrome105870790.
- Aase_syndrome type Syndromes.
- Aase_syndrome type Whole105869584.
- Aase_syndrome type Disease.
- Aase_syndrome type AilmentCondition.
- Aase_syndrome type Situation.
- Aase_syndrome comment "Aase syndrome or Aase–Smith syndrome is a rare inherited disorder characterized by anemia with some joint and skeletal deformities. Aase syndrome is thought to be an autosomal recessive inherited disorder. The genetic basis of the disease is not known. The anemia is caused by underdevelopment of the bone marrow, which is where blood cells are formed.It is named after the American paediatricians Jon Morton Aase and David Weyhe Smith, who characterized it in 1968.".
- Aase_syndrome label "Aase syndrome".
- Aase_syndrome label "Sindrome di Aase-Smith".
- Aase_syndrome label "Syndrome d'Aase".
- Aase_syndrome label "Síndrome de Aase".
- Aase_syndrome label "Síndrome de Aase".
- Aase_syndrome label "Zespół Aase'a".
- Aase_syndrome label "متلازمة آس".
- Aase_syndrome sameAs Síndrome_de_Aase.
- Aase_syndrome sameAs Syndrome_d'Aase.
- Aase_syndrome sameAs Sindrom_Aase.
- Aase_syndrome sameAs Sindrome_di_Aase-Smith.
- Aase_syndrome sameAs Zespół_Aase'a.
- Aase_syndrome sameAs Síndrome_de_Aase.
- Aase_syndrome sameAs m.048h6d.
- Aase_syndrome sameAs Q1441838.
- Aase_syndrome sameAs Q1441838.
- Aase_syndrome sameAs Aase_syndrome.
- Aase_syndrome wasDerivedFrom Aase_syndrome?oldid=560019878.
- Aase_syndrome isPrimaryTopicOf Aase_syndrome.
- Aase_syndrome name "Aase syndrome".