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Environmental Biomarkers
|
D23.101.258 |
|
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Trypanosoma
|
B01.268.475.868.887 |
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Leukosialin
|
D12.776.395.560.631.650.143 |
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Sialomucins
|
D12.776.395.560.631.650 |
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Enclomiphene
|
D02.455.426.559.389.150.700.125.500 |
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Melissa
|
B01.650.940.800.575.912.250.583.520.474 |
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Insulin-Like Growth Factor Binding Protein 5
|
D12.776.157.420.290 |
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Zantedeschia
|
D031064 |
[A plant genus of the family ARACEAE. The common name of Calla Lily or Callalily also refers to the Calla genus (CALLA PLANT).
] |
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Primary Graft Dysfunction
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D055031 |
[A form of ischemia-reperfusion injury occurring in the early period following transplantation. Significant pathophysiological changes in MITOCHONDRIA are the main cause of the dysfunction. It is most often seen in the transplanted lung, liver, or kidney and can lead to GRAFT REJECTION.
] |
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Electron Microscope Tomography
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D055032 |
[A tomographic technique for obtaining 3-dimensional images with transmission electron microscopy.
] |
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Meningocele
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C10.500.680.598 |
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Pneumonia, Lipid
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C01.748.610.529.612 |
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Drug Users
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D055030 |
[People who take drugs for a non-therapeutic or non-medical effect. The drugs may be legal or illegal, but their use often results in adverse medical, legal, or social consequences for the users.
] |
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Sarcoma, Kaposi
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C04.557.645.750 |
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Colocasia
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D031060 |
[A plant genus of the family ARACEAE. Members contain acrid calcium oxalate and LECTINS. Polynesians prepare the root into poi. Common names of Taro and Coco Yam (Cocoyam) may be confused with other ARACEAE; XANTHOSOMA; or with common yam (DIOSCOREA).
] |
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Gout
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C18.452.648.798.368 |
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Purine-Pyrimidine Metabolism, Inborn Errors
|
C18.452.648.798 |
|
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Spinal Osteochondrosis
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D055035 |
[A bone disorder involving ossification centers (EPIPHYSES) of the VERTEBRAL COLUMN.
] |
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Cyrtosperma
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D031061 |
[A plant genus of the family ARACEAE that may be confused with other ARACEAE having similar common names.
] |
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Campomelic Dysplasia
|
D055036 |
[A rarer variant of campomelic dysplasia. The characteristics match campomelic dysplasia except that long bone curvature is not present (acampomelia).
, A congenital disorder of CHONDROGENESIS and OSTEOGENESIS characterized by hypoplasia of endochondral bones. In most cases there is a curvature of the long bones especially the TIBIA with dimpling of the skin over the bowed areas, malformation of the pelvis and spine, 11 pairs of ribs, hypoplastic scapulae, club feet, micrognathia, CLEFT PALATE, tracheobronchomalacia, and in some patients male-to-female sex reversal (SEX REVERSAL, GONADAL). Most patients die in the neonatal period of respiratory distress. Campomelic dysplasia is associated with haploinsufficiency of the SOX9 TRANSCRIPTION FACTOR gene.
] |
