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Prader-Willi syndrome
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
NDN
SNRPN
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
BRIDEAU_IMPRINTED_GENES
GSE14308_TH2_VS_NATURAL_TREG_UP
Necdin
Small ribonucleoprotein associated, SmB/SmN
RCGCANGCGY_NRF1_Q6
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Curated Studies
Most Correlated Studies
Brains and skeletal muscles of Prader-Will syndrome imprinting center (PWS-IC) deleted mice
Induced pluripotent stem cells (iPSCs) and fibroblasts of patients with Prader-Willi syndrome
Neurons CD56+ from iPSCs of Prader-Willi syndrome patients with chromosome 15q deletion
Mouse Phenotypes - Anomaly of chromosome pair 15
OMIM - Congenital disorder
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Literature
Most Relevant Literature
Are sleep studies helpful in children with Prader-Willi syndrome prior to commencement of growth hor…
Regional cerebral blood flow and abnormal eating behavior in Prader-Willi syndrome.
Risk for ingestion of toxic substances in children with Prader-Willi syndrome.
GrowthHormone Research Society workshop summary: consensus guidelines for recombinant human growth h…
Longitudinal evaluation of sleep-disordered breathing in children with Prader-Willi Syndrome during …
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Clinical Trials
Most Relevant Clinical Trials
Hypoglycemia in Prader-Willi Syndrome
Autonomic Regulation in Prader-Willi Syndrome
Liraglutide Use in Prader-Willi Syndrome
Oxytocin Trial in Prader-Willi Syndrome
Probiotic Treatment for Prader-Willi Syndrome
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