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

ENSG00000087460 - GNAS complex locus

Gene

ENSG00000100292 - heme oxygenase 1

Gene

ENSG00000107984 - dickkopf Wnt signaling pathway inhibitor 1

Gene

ENSG00000197249 - serpin family A member 1

Gene

ENSG00000197172 - MAGE family member A6

Gene

ENSG00000086548 - CEA cell adhesion molecule 6

Gene

ENSG00000164120 - 15-hydroxyprostaglandin dehydrogenase

Gene

ENSG00000125398 - SRY-box transcription factor 9

Gene

ENSG00000128422 - keratin 17

Gene

ENSG00000244734 - hemoglobin subunit beta

  • Gene

    ENSG00000087460 - GNAS complex locus


  • Gene

    ENSG00000100292 - heme oxygenase 1


  • Gene

    ENSG00000107984 - dickkopf Wnt signaling pathway inhibitor 1


  • Gene

    ENSG00000197249 - serpin family A member 1


  • Gene

    ENSG00000197172 - MAGE family member A6


  • Gene

    ENSG00000086548 - CEA cell adhesion molecule 6


  • Gene

    ENSG00000164120 - 15-hydroxyprostaglandin dehydrogenase


  • Gene

    ENSG00000125398 - SRY-box transcription factor 9


  • Gene

    ENSG00000128422 - keratin 17


  • Gene

    ENSG00000244734 - hemoglobin subunit beta

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