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🏥 Disease / Health Topic

Prader-Willi Syndrome

8
Clinical Trials
1
Meta-Analyses
0
PubMed References
📋 Sample Trials
NCT02629991
Oxytocin vs. Placebo for the Treatment Hyperphagia in Children and Adolescents With Prader-Willi Syndrome
Completed · Phase 2
NCT02804373
Effects of Intranasal Administration of Oxytocin in Adults With Prader-Willi Syndrome
Completed · Phase 2|Phase 3
NCT03114371
Oxytocin Intranasal Administrations in Children With Prader-Willi Syndrome Aged From 3 to 12 Years
Completed
📊 Sample Meta-Analyses
CRD42020220646
The effects of oxytocin and its analog, carbetocin, on hyperphagia and behavioral disorders in patients with Prader-Willi Syndrome
Prader-Willi Syndrome (PWS) is a rare, complex and multisystemic genetic disorde
📚 Sample References
None linked yet.
🏥 All Disease / Health Topic data fields for Prader-Willi Syndrome
🏥 Names
Disease Name
Prader-Willi Syndrome
Alias Names
Noonan Syndrome; Prader-Willi Syndrome; Cornelia De Lange Syndrome; Noonan Syndrome 5; Noonan Syndrome 10; Microcephalic Osteodysplastic Primordial Dwarfism Type Ii; Noonan Syndrome 2; Royer Syndrome; Dubowitz Syndrome; Silver-Russell Syndrome; Seckel Syndrome; Noonan Syndrome 7; Noonan Syndrome 3; Cockayne Syndrome; Noonan Syndrome 4; Aarskog Syndrome; Noonan Syndrome 8; Microcephalic Osteodysplastic Primordial Dwarfism Type I; Noonan Syndrome 6; Noonan Syndrome 1; Noonan Syndrome 9
Topic Type
syndrome
🧬 Ontology Classifications
DisGeNET Type
disease
UMLS Type
Disease or Syndrome
MeSH Class
Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
DO Class
disease of mental health; disease of anatomical entity; genetic disease; syndrome
🔗 External References
Disease Ontology
60609; 60580; 2962; 14796; 3490;
DisGeNET
C0032897
🔍 Raw view — every non-empty column on this row (27 fields)
name
Prader-Willi Syndrome
alias name
Noonan Syndrome; Prader-Willi Syndrome; Cornelia De Lange Syndrome; Noonan Syndrome 5; Noonan Syndrome 10; Microcephalic Osteodysplastic Primordial Dwarfism Type Ii; Noonan Syndrome 2; Royer Syndrome; Dubowitz Syndrome; Silver-Russell Syndrome; Seckel Syndrome; Noonan Syndrome 7; Noonan Syndrome 3; Cockayne Syndrome; Noonan Syndrome 4; Aarskog Syndrome; Noonan Syndrome 8; Microcephalic Osteodysplastic Primordial Dwarfism Type I; Noonan Syndrome 6; Noonan Syndrome 1; Noonan Syndrome 9
topic type
syndrome
disgenet disease type
disease
umls disease type
Disease or Syndrome
mesh disease class
Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
do disease class
disease of mental health; disease of anatomical entity; genetic disease; syndrome
umls disease type id
T047
mesh disease class id
C16; C10; C18
do disease class id
DOID:150; DOID:7; DOID:225; DOID
herb disease id
HBDIS002458
disgenet id
C0032897
mesh id
D011218
do id
60609; 60580; 2962; 14796; 3490;
omim id
176270

⚗️ Related Ingredients

1 · compounds in this herb

📋 Clinical Trials

8 · subject of clinical study
NCT02629991 Oxytocin vs. Placebo for the Treatment Hyperphagia in Children and Adolescents W
→ Prader-Willi Syndrome|Hyperphagia
NCT02804373 Effects of Intranasal Administration of Oxytocin in Adults With Prader-Willi Syn
→ Prader-Willi Syndrome
NCT03114371 Oxytocin Intranasal Administrations in Children With Prader-Willi Syndrome Aged
→ Prader-Willi Syndrome
NCT03197662 Intranasal Oxytocin vs. Placebo for the Treatment of Hyperphagia in Prader-Willi
→ Prader-Willi Syndrome|Hyperphagia
NCT03245762 Intranasal Oxytocin for Infants With Prader-Willi Syndrome
→ Prader-Willi Syndrome
NCT03081832 Follow-up of Prader Willi Syndrome Infants Treated by Oxytocin and Comparison Wi
→ Prader-Willi Syndrome
NCT04283578 Oxytocin Treatment in Neonates and Infants With Prader-Willi Syndrome
→ Prader-Willi Syndrome
NCT05298085 Effect of Intranasal Oxytocin on Dysphagia in Children and Adolescents With Prad
→ Prader-Willi Syndrome

📊 Meta-Analyses

1 · systematic review
CRD42020220646 The effects of oxytocin and its analog, carbetocin, on hyperphagia and behaviora
→ Prader-Willi Syndrome (PWS) is a rare, complex and
How relationships are computed
  • Clinical Trials / Meta-Analyses / References: direct foreign-key link via subject_entity_id (Phase 2d wireup)
  • Formula ↔ Herbs: text bridge via formulas.herbs_in_pinyin matching herbs.pinyin_name
  • Herb ↔ Ingredient: ACTIVE — direct link via herb_ingredients
  • Ingredient ↔ Target: ACTIVE — direct link via ingredient_targets
  • Target ↔ Disease: ACTIVE — direct link via target_health_topics
  • Herb → Target → Disease (full chemical spine): ACTIVE — joins all three link tables