ib – -Translation – Keybot Dictionary

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  Isolated growth hormone...  
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Isolated growth hormone deficiency type IB ( Congenital IGHD type IB Congenital isolated GH deficiency type IB Congenital isolated growth hormone deficiency type IB )
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Deficit isolato dell'ormone della crescita, tipo 1B ( Deficit isolato congenito dell'ormone della crescita, tipo 1B Deficit isolato congenito di GH, tipo 1B IGHD congenito, tipo 1B )
  MPI-CDG | aidWeb  
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MPI-CDG ( CDG syndrome type Ib CDG-Ib CDG1B Carbohydrate deficient glycoprotein syndrome type Ib Congenital disorder of glycosylation type 1b Congenital disorder of glycosylation type Ib Phosphomannose isomerase deficiency )
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Sindrome MPI-CDG ( CDG-Ib CDG1B Deficit di fosfomannosio isomerasi Disturbo congenito della glicosilazione, tipo 1b Disturbo congenito della glicosilazione, tipo Ib Sindrome CDG, tipo Ib Sindrome delle glicoproteine carenti in carboidrati, tipo Ib )
  MPI-CDG | aidWeb  
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MPI-CDG ( CDG syndrome type Ib CDG-Ib CDG1B Carbohydrate deficient glycoprotein syndrome type Ib Congenital disorder of glycosylation type 1b Congenital disorder of glycosylation type Ib Phosphomannose isomerase deficiency )
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Sindrome MPI-CDG ( CDG-Ib CDG1B Deficit di fosfomannosio isomerasi Disturbo congenito della glicosilazione, tipo 1b Disturbo congenito della glicosilazione, tipo Ib Sindrome CDG, tipo Ib Sindrome delle glicoproteine carenti in carboidrati, tipo Ib )
  Bernard-Soulier syndrom...  
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The gene involved is glycoprotein Ib (platelet), alpha polypeptide ("GP1BA")
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Il gene coinvolto è glycoprotein Ib (platelet), alpha polypeptide ("GP1BA")
  Acromesomelic dysplasia...  
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The gene involved is bone morphogenetic protein receptor, type IB ("BMPR1B")
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Il gene coinvolto è bone morphogenetic protein receptor, type IB ("BMPR1B")
  MPI-CDG | aidWeb  
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MPI-CDG ( CDG syndrome type Ib CDG-Ib CDG1B Carbohydrate deficient glycoprotein syndrome type Ib Congenital disorder of glycosylation type 1b Congenital disorder of glycosylation type Ib Phosphomannose isomerase deficiency )
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Sindrome MPI-CDG ( CDG-Ib CDG1B Deficit di fosfomannosio isomerasi Disturbo congenito della glicosilazione, tipo 1b Disturbo congenito della glicosilazione, tipo Ib Sindrome CDG, tipo Ib Sindrome delle glicoproteine carenti in carboidrati, tipo Ib )
  Isolated growth hormone...  
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Isolated growth hormone deficiency type IB
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Deficit isolato dell'ormone della crescita, tipo 1B
  Isolated growth hormone...  
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Isolated growth hormone deficiency type IB ( Congenital IGHD type IB Congenital isolated GH deficiency type IB Congenital isolated growth hormone deficiency type IB )
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Deficit isolato dell'ormone della crescita, tipo 1B ( Deficit isolato congenito dell'ormone della crescita, tipo 1B Deficit isolato congenito di GH, tipo 1B IGHD congenito, tipo 1B )
  Isolated growth hormone...  
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Isolated growth hormone deficiency type IB ( Congenital IGHD type IB Congenital isolated GH deficiency type IB Congenital isolated growth hormone deficiency type IB )
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Deficit isolato dell'ormone della crescita, tipo 1B ( Deficit isolato congenito dell'ormone della crescita, tipo 1B Deficit isolato congenito di GH, tipo 1B IGHD congenito, tipo 1B )
  Isolated growth hormone...  
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Isolated growth hormone deficiency type IB ( Congenital IGHD type IB Congenital isolated GH deficiency type IB Congenital isolated growth hormone deficiency type IB )
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Deficit isolato dell'ormone della crescita, tipo 1B ( Deficit isolato congenito dell'ormone della crescita, tipo 1B Deficit isolato congenito di GH, tipo 1B IGHD congenito, tipo 1B )
  Isolated focal cortical...  
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Isolated focal cortical dysplasia type Ib ( FCD type Ib )
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Displasia corticale focale isolata, tipo Ib ( FCD, tipo Ib )
  Isolated focal cortical...  
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Isolated focal cortical dysplasia type Ib
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Displasia corticale focale isolata, tipo Ib
  Isolated focal cortical...  
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Isolated focal cortical dysplasia type Ib ( FCD type Ib )
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Displasia corticale focale isolata, tipo Ib ( FCD, tipo Ib )
  MPI-CDG | aidWeb  
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MPI-CDG ( CDG syndrome type Ib CDG-Ib CDG1B Carbohydrate deficient glycoprotein syndrome type Ib Congenital disorder of glycosylation type 1b Congenital disorder of glycosylation type Ib Phosphomannose isomerase deficiency )
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Sindrome MPI-CDG ( CDG-Ib CDG1B Deficit di fosfomannosio isomerasi Disturbo congenito della glicosilazione, tipo 1b Disturbo congenito della glicosilazione, tipo Ib Sindrome CDG, tipo Ib Sindrome delle glicoproteine carenti in carboidrati, tipo Ib )
  Glycogen storage diseas...  
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Glycogen storage disease due to glucose-6-phosphatase deficiency type b ( G6P deficiency type b G6P translocase deficiency G6PT deficiency GSD due to G6P deficiency type b GSD due to G6PT deficiency GSD type 1 non a GSD type 1b GSDIb Glycogen storage disease due to G6P deficiency type b Glycogen storage disease type 1b Glycogenosis due to glucose-6-phosphatase deficiency type b Glycogenosis due to glucose-6-phosphatase transport defect Glycogenosis type Ib )
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Malattia da deposito di glicogeno dovuta a deficit di glucosio-6-fosfatasi, tipo b ( Deficit di G6P translocasi Deficit di G6P, tipo b Deficit di G6PT GSD da deficit di G6P, tipo b GSD da deficit di G6PT GSD da deficit diG6PT GSD, tipo 1 non-a GSD, tipo 1b GSDIb Glicogenosi Ib Glicogenosi da deficit di glucosio-6-fosfatasi, tipo b Glicogenosi da difetto del trasporto di glucosio-6-fosfatasi Glicogenosi, tipo Ib Malattia da deposito di glicogeno dovuta a deficit di G6P, tipo b Malattia da deposito di glicogeno, tipo 1b )