EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.7.1.30 | Adenoma |
194794 |
Glycerol kinase activity in adenoma alveolar type II cells. |
ongoing research
therapeutic application
unassigned |
4
1
0 |
| 2.7.1.30 | Adrenal Insufficiency |
2550352 |
Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locus. |
causal interaction
unassigned |
1
0 |
| 2.7.1.30 | Adrenal Insufficiency |
2828063 |
Infantile glycerol kinase deficiency--a condition requiring prompt identification. Clinical, biochemical, and morphological findings in two cases. |
causal interaction
unassigned |
4
0 |
| 2.7.1.30 | Adrenal Insufficiency |
2906226 |
Congenital adrenal hypoplasia and selective absence of pituitary luteinizing hormone: a new autosomal recessive syndrome. |
causal interaction
unassigned |
4
0 |
| 2.7.1.30 | Adrenal Insufficiency |
3003318 |
Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion. |
causal interaction
ongoing research
unassigned |
4
1
0 |
| 2.7.1.30 | Adrenal Insufficiency |
3027343 |
Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies. |
causal interaction
diagnostic usage
unassigned |
4
3
0 |
| 2.7.1.30 | Adrenal Insufficiency |
6249182 |
Glycerol kinase deficiency with neuromuscular, skeletal, and adrenal abnormalities. |
causal interaction
unassigned |
4
0 |
| 2.7.1.30 | Adrenal Insufficiency |
7512107 |
Isolated glycerol kinase deficiency in a neonate. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.7.1.30 | Adrenal Insufficiency |
7955386 |
Congenital adrenal hypoplasia, Duchenne muscular dystrophy, and glycerol kinase deficiency: importance of laboratory investigations in delineating a contiguous gene deletion syndrome. |
causal interaction
therapeutic application
unassigned |
2
1
0 |
| 2.7.1.30 | Albinism |
2227145 |
Old syndromes and new cytogenetics. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
