Osteoporosis (Phenotype)

Synonyms:HP:0002774
Id:HP:0000939
Description:Osteoporosis is a systemic skeletal disease characterized by low bone density and microarchitectural deterioration of bone tissue with a consequent increase in bone fragility. According to the WHO criteria, osteoporosis is defined as a BMD that lies 2.5 standard deviations or more below the average value for young healthy adults (a T-score below -2.5 SD).
Results found

Linked to

 

Label

Description

 

Gene

GNAS complex locus

Gene

MAGE family member A6

Gene

serpin family A member 1

Gene

IKAROS family zinc finger 1

Gene

dickkopf Wnt signaling pathway inhibitor 1

Gene

CEA cell adhesion molecule 6

Gene

15-hydroxyprostaglandin dehydrogenase

Gene

hemoglobin subunit beta

Gene

SRY-box transcription factor 9

Gene

SRC proto-oncogene, non-receptor tyrosine kinase

  • Gene

    GNAS complex locus


  • Gene

    MAGE family member A6


  • Gene

    serpin family A member 1


  • Gene

    IKAROS family zinc finger 1


  • Gene

    dickkopf Wnt signaling pathway inhibitor 1


  • Gene

    CEA cell adhesion molecule 6


  • Gene

    15-hydroxyprostaglandin dehydrogenase


  • Gene

    hemoglobin subunit beta


  • Gene

    SRY-box transcription factor 9


  • Gene

    SRC proto-oncogene, non-receptor tyrosine kinase

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