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- Hypochondroplasia abstract "Hypochondroplasia is a developmental disorder caused by an autosomal dominant genetic defect in the fibroblast growth factor receptor 3 gene (FGFR3) that results in a disproportionately short stature, micromelia, and a head that appears large when compared with the underdeveloped portions of the body. It is also known as "achondroplasia tarda" and "atypical achondroplasia."It is classified as short-limbed dwarfism.".
- Hypochondroplasia diseasesdb "32832".
- Hypochondroplasia icd10 "Q77.4".
- Hypochondroplasia omim "146000".
- Hypochondroplasia wikiPageExternalLink NBK1477.
- Hypochondroplasia wikiPageID "2950938".
- Hypochondroplasia wikiPageRevisionID "591196728".
- Hypochondroplasia diseasesdb "32832".
- Hypochondroplasia genereviewsname "Hypochondroplasia".
- Hypochondroplasia genereviewsnbk "NBK1477".
- Hypochondroplasia hasPhotoCollection Hypochondroplasia.
- Hypochondroplasia icd "Q77.4".
- Hypochondroplasia name "Hypochondroplasia".
- Hypochondroplasia omim "146000".
- Hypochondroplasia wordnet_type synset-disease-noun-1.
- Hypochondroplasia subject Category:Cell_surface_receptor_deficiencies.
- Hypochondroplasia subject Category:Growth_disorders.
- Hypochondroplasia subject Category:Skeletal_system.
- Hypochondroplasia type Abstraction100002137.
- Hypochondroplasia type Attribute100024264.
- Hypochondroplasia type CellSurfaceReceptorDeficiencies.
- Hypochondroplasia type Condition113920835.
- Hypochondroplasia type Disease114070360.
- Hypochondroplasia type Disorder114052403.
- Hypochondroplasia type GrowthDisorders.
- Hypochondroplasia type IllHealth114052046.
- Hypochondroplasia type Illness114061805.
- Hypochondroplasia type Lack114449405.
- Hypochondroplasia type Need114449126.
- Hypochondroplasia type PathologicalState114051917.
- Hypochondroplasia type PhysicalCondition114034177.
- Hypochondroplasia type State100024720.
- Hypochondroplasia type Disease.
- Hypochondroplasia type AilmentCondition.
- Hypochondroplasia type Situation.
- Hypochondroplasia comment "Hypochondroplasia is a developmental disorder caused by an autosomal dominant genetic defect in the fibroblast growth factor receptor 3 gene (FGFR3) that results in a disproportionately short stature, micromelia, and a head that appears large when compared with the underdeveloped portions of the body. It is also known as "achondroplasia tarda" and "atypical achondroplasia."It is classified as short-limbed dwarfism.".
- Hypochondroplasia label "Hipochondroplazja".
- Hypochondroplasia label "Hipocondroplasia".
- Hypochondroplasia label "Hipocondroplasia".
- Hypochondroplasia label "Hypochondroplasia".
- Hypochondroplasia label "Hypochondroplasie".
- Hypochondroplasia label "Hypochondroplasie".
- Hypochondroplasia label "季肋發育不全".
- Hypochondroplasia sameAs Hypochondroplasie.
- Hypochondroplasia sameAs Hipocondroplasia.
- Hypochondroplasia sameAs Hypochondroplasie.
- Hypochondroplasia sameAs Hipochondroplazja.
- Hypochondroplasia sameAs Hipocondroplasia.
- Hypochondroplasia sameAs m.08fpcb.
- Hypochondroplasia sameAs Q1283054.
- Hypochondroplasia sameAs Q1283054.
- Hypochondroplasia sameAs 573.
- Hypochondroplasia sameAs Hypochondroplasia.
- Hypochondroplasia wasDerivedFrom Hypochondroplasia?oldid=591196728.
- Hypochondroplasia isPrimaryTopicOf Hypochondroplasia.
- Hypochondroplasia name "Hypochondroplasia".