|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Induced microseizures in West syndrome.
|
1656808 |
1991 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Induced microseizures in West syndrome.
|
1656808 |
1991 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
[Cardiac hypertrophy associated with subaortic obstruction induced by adrenocorticotropic hormone treatment].
|
1965992 |
1990 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
[Cardiac hypertrophy associated with subaortic obstruction induced by adrenocorticotropic hormone treatment].
|
1965992 |
1990 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Hormonal background of the hypertension and fluid derangements associated with adrenocorticotrophic hormone treatment of infants.
|
2551692 |
1989 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
ACTH-induced seizures in an infant with West syndrome.
|
2554740 |
1989 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Hormonal background of the hypertension and fluid derangements associated with adrenocorticotrophic hormone treatment of infants.
|
2551692 |
1989 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
ACTH-induced seizures in an infant with West syndrome.
|
2554740 |
1989 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
[Secondary myocardial hypertrophy in newborn infants and infants without congenital heart defect].
|
2853496 |
1988 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
[Secondary myocardial hypertrophy in newborn infants and infants without congenital heart defect].
|
2853496 |
1988 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
[How effective is the treatment schedule in children with infantile spasms?].
|
2983143 |
1985 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
[How effective is the treatment schedule in children with infantile spasms?].
|
2983143 |
1985 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Renal and pancreatic calcification during treatment of infantile spasms with ACTH.
|
6143199 |
1984 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Renal and pancreatic calcification during treatment of infantile spasms with ACTH.
|
6143199 |
1984 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Long-term prognosis after infantile spasms: a statistical study of prognostic factors in 200 cases.
|
6259007 |
1981 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Long-term prognosis after infantile spasms: a statistical study of prognostic factors in 200 cases.
|
6259007 |
1981 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
[Lethal side effects from ACTH-therapy in infantile spasm (author's transl)].
|
6107850 |
1980 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
[Lethal side effects from ACTH-therapy in infantile spasm (author's transl)].
|
6107850 |
1980 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
ACTH therapy in infantile spasms: side effects.
|
6254450 |
1980 |
|
| Entrez Id: |
5443 |
| Gene Symbol: |
POMC |
POMC
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
ACTH therapy in infantile spasms: side effects.
|
6254450 |
1980 |
|
| Entrez Id: |
7355 |
| Gene Symbol: |
SLC35A2 |
SLC35A2
|
0.100 |
GeneticVariation
|
phenotype |
CLINVAR |
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals.
|
30817854 |
2019 |
|
| Entrez Id: |
547 |
| Gene Symbol: |
KIF1A |
KIF1A
|
0.100 |
CausalMutation
|
phenotype |
CLINVAR |
De novo dominant variants affecting the motor domain of KIF1A are a cause of PEHO syndrome.
|
26486474 |
2016 |
|
| Entrez Id: |
55780 |
| Gene Symbol: |
ERMARD |
ERMARD
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
6487 |
| Gene Symbol: |
ST3GAL3 |
ST3GAL3
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
|
| Entrez Id: |
8831 |
| Gene Symbol: |
SYNGAP1 |
SYNGAP1
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|