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Gene Information
Gene symbol: BTD
Gene name: biotinidase
HGNC ID: 1122
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | ALB | 1 hits |
| 2 | HEXA | 1 hits |
| 3 | HLCS | 1 hits |
| 4 | INS | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 9156561 | Urinary biotinidase and alanine excretion in patients with insulin-dependent diabetes mellitus. |
| 2 | 9156561 | Twenty-four-hour urine specimens from 21 juvenile insulin-dependent diabetics and 10 healthy controls were compared with respect to biotinidase activity and alanine content. |
| 3 | 9156561 | Biotinidase excretion in diabetics was correlated with alanine excretion (rS = 0.667; p < 0.01), but not with protein, albumin or N-acetyl-beta-glucosaminidase excretion. |
| 4 | 9156561 | Urinary biotinidase and alanine excretion in patients with insulin-dependent diabetes mellitus. |
| 5 | 9156561 | Twenty-four-hour urine specimens from 21 juvenile insulin-dependent diabetics and 10 healthy controls were compared with respect to biotinidase activity and alanine content. |
| 6 | 9156561 | Biotinidase excretion in diabetics was correlated with alanine excretion (rS = 0.667; p < 0.01), but not with protein, albumin or N-acetyl-beta-glucosaminidase excretion. |
| 7 | 9156561 | Urinary biotinidase and alanine excretion in patients with insulin-dependent diabetes mellitus. |
| 8 | 9156561 | Twenty-four-hour urine specimens from 21 juvenile insulin-dependent diabetics and 10 healthy controls were compared with respect to biotinidase activity and alanine content. |
| 9 | 9156561 | Biotinidase excretion in diabetics was correlated with alanine excretion (rS = 0.667; p < 0.01), but not with protein, albumin or N-acetyl-beta-glucosaminidase excretion. |
| 10 | 15095958 | Multiple carboxylase deficiency (MCD) is a rare inherited metabolic disease of biotin dependency due to deficiency of holocarboxylase synthetase (HCS) or biotinidase deficiency. |
| 11 | 23622402 | Two inherited defects in biotin metabolism are known, holocarboxylase synthetase and biotinidase deficiency. |