EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   4.4.1.17 | Cerebral Palsy |
28587475 |
Management of Severe Equinovalgus in Patients With Cerebral Palsy by Naviculectomy in Combination With Midfoot Arthrodesis. |
unassigned |
0 |
| 4.4.1.17 | Erythema |
7096664 |
Psoralen-containing sunscreen induces phototoxicity and epidermal ornithine decarboxylase activity. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
4
1
0 |
| 4.4.1.17 | Hernias, Diaphragmatic, Congenital |
20503342 |
Deletions of Xp provide evidence for the role of holocytochrome C-type synthase (HCCS) in congenital diaphragmatic hernia. |
causal interaction
unassigned |
1
0 |
| 4.4.1.17 | Hyperglycemia |
24822205 |
The impact of hyperglycemia on risk of severe infections during early period of induction therapy in patients with newly diagnosed multiple myeloma. |
diagnostic usage
unassigned |
3
0 |
| 4.4.1.17 | Infections |
24822205 |
The impact of hyperglycemia on risk of severe infections during early period of induction therapy in patients with newly diagnosed multiple myeloma. |
diagnostic usage
unassigned |
3
0 |
| 4.4.1.17 | Lymphopenia |
24822205 |
The impact of hyperglycemia on risk of severe infections during early period of induction therapy in patients with newly diagnosed multiple myeloma. |
diagnostic usage
unassigned |
3
0 |
| 4.4.1.17 | Melanoma |
30721686 |
The Lens Opacities Classification System III grading in irradiated uveal melanomas to characterize proton induced cataracts. |
diagnostic usage
unassigned |
2
0 |
| 4.4.1.17 | Microphthalmos |
15576047 |
Defects in the biosynthesis of mitochondrial heme c and heme a in yeast and mammals. |
causal interaction
unassigned |
4
0 |
| 4.4.1.17 | Microphthalmos |
17033964 |
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome. |
unassigned |
0 |
| 4.4.1.17 | Microphthalmos |
17893649 |
HCCS loss-of-function missense mutation in a female with bilateral microphthalmia and sclerocornea: a novel gene for severe ocular malformations? |
causal interaction
unassigned |
4
0 |
