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Results 1 - 10 of 51 for IBS
  1. GP1BB gene 
    ... Condition antigen CD42b-beta BDPLT1 BS CD42C glycoprotein Ib (platelet), beta polypeptide glycoprotein Ib platelet beta subunit GP-Ib beta GPIBB GPIbbeta ...
    https://medlineplus.gov/genetics/gene/gp1bb - Genetics
  2. GP1BA gene 
    ... provides instructions for making a protein called glycoprotein Ib-alpha (GPIbα). This protein is one piece (subunit) ... BDPLT1 BDPLT3 BSS CD42B CD42b-alpha DBPLT3 glycoprotein Ib (platelet), alpha polypeptide glycoprotein Ib platelet alpha subunit ...
    https://medlineplus.gov/genetics/gene/gp1ba - Genetics
  3. Bernard-Soulier syndrome 
    ... subunits) of a protein complex called glycoprotein (GP)Ib-IX-V. This complex is found on the ... of platelet glycoprotein 1b Giant platelet syndrome Glycoprotein Ib, platelet, deficiency of Hemorrhagioparous thrombocytic dystrophy Macrothrombocytopenia, familial ...
    https://medlineplus.gov/genetics/condition/bernard-soulier-syndrome - Genetics
  4. PAFAH1B1 gene 
    ... subunit 1 (45kDa) platelet-activating factor acetylhydrolase, isoform Ib, alpha subunit platelet-activating factor acetylhydrolase, isoform Ib, subunit 1 (45kDa) Tests of PAFAH1B1 PubMed PLATELET- ...
    https://medlineplus.gov/genetics/gene/pafah1b1 - Genetics
  5. Isolated growth hormone deficiency 
    ... birth.People with isolated growth hormone deficiency type IB produce very low levels of growth hormone. As a result, type IB is characterized by short stature, but this growth ...
    https://medlineplus.gov/.../isolated-growth-hormone-deficiency - Genetics
  6. Progressive familial heart block 
    ... I being further divided into types IA and IB. These types differ in where in the heart ... and the genetic cause. In types IA and IB, the heart block originates in the bundle branch, ...
    https://medlineplus.gov/.../progressive-familial-heart-block - Genetics
  7. Glycogen storage disease type I 
    ... type Ia (GSDIa) and glycogen storage disease type Ib (GSDIb). Two other forms of GSDI have been ... disease due to glucose-6-phosphatase deficiency type Ib National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-i - Genetics
  8. Aicardi syndrome 
    ... W, Lewis RA, Fang P, Van den Veyver IB. Non-random X chromosome inactivation in Aicardi syndrome. ... Lewis RA, Park Parsons D, Van den Veyver IB. Phenotype and management of Aicardi syndrome: new findings ...
    https://medlineplus.gov/genetics/condition/aicardi-syndrome - Genetics
  9. GP9 gene 
    ... Ran Y, Lopez JA, Peng Y. Platelet glycoprotein Ib beta/IX mediates glycoprotein Ib alpha localization to membrane lipid domain critical for ... J. The organizing principle of the platelet glycoprotein Ib-IX-V complex. J Thromb Haemost. 2013 Apr; ...
    https://medlineplus.gov/genetics/gene/gp9 - Genetics
  10. Achondrogenesis 
    ... Achondrogenesis, type IA Genetic Testing Registry: Achondrogenesis, type IB Achondrogenesis National Organization for Rare Disorders (NORD) ACHONDROGENESIS, ...
    https://medlineplus.gov/genetics/condition/achondrogenesis - Genetics
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