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Ingredient
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Gene Target
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Disease
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Evidence
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trials · metas · refs
Plus 6,743 TCM formulas connecting herbs together
🏥 Disease / Health Topic
Osteogenesis Imperfecta
0
Clinical Trials
0
Meta-Analyses
0
PubMed References
🏥 All Disease / Health Topic data fields for Osteogenesis Imperfecta
🏥 Names
Disease Name
Osteogenesis Imperfecta
Alias Names
Osteogenesis Imperfecta Type 6; Osteogenesis Imperfecta Type 2; Osteogenesis Imperfecta Type 15; Osteogenesis Imperfecta Type 12; Osteogenesis Imperfecta Type 14; Osteogenesis Imperfecta Type 8; Osteogenesis Imperfecta Type 4; Osteogenesis Imperfecta Type 5; Osteogenesis Imperfecta Type 3; Osteogenesis Imperfecta Type 10; Osteogenesis Imperfecta; Osteogenesis Imperfecta Type 1; Osteogenesis Imperfecta Type 9; Lobstein Disease; Osteogenesis Imperfecta Type 16; Osteogenesis Imperfecta Type 7; Oste
Topic Type
syndrome
🧬 Ontology Classifications
DisGeNET Type
disease
UMLS Type
Disease or Syndrome; Congenital Abnormality
MeSH Class
Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
DO Class
disease of anatomical entity; genetic disease
🔗 External References
HERB DB
MeSH
ICD-10
Disease Ontology
110334; 110342; 110341; 110337;
DisGeNET
C0029434
🔍 Raw view — every non-empty column on this row (27 fields)
name
Osteogenesis Imperfecta
alias name
Osteogenesis Imperfecta Type 6; Osteogenesis Imperfecta Type 2; Osteogenesis Imperfecta Type 15; Osteogenesis Imperfecta Type 12; Osteogenesis Imperfecta Type 14; Osteogenesis Imperfecta Type 8; Osteogenesis Imperfecta Type 4; Osteogenesis Imperfecta Type 5; Osteogenesis Imperfecta Type 3; Osteogenesis Imperfecta Type 10; Osteogenesis Imperfecta; Osteogenesis Imperfecta Type 1; Osteogenesis Imperfecta Type 9; Lobstein Disease; Osteogenesis Imperfecta Type 16; Osteogenesis Imperfecta Type 7; Osteogenesis Imperfecta Type 11; Osteogenesis Imperfecta Type 17; Osteogenesis Imperfecta With Opalescen
topic type
syndrome
disgenet disease type
disease
umls disease type
Disease or Syndrome; Congenital Abnormality
mesh disease class
Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
do disease class
disease of anatomical entity; genetic disease
umls disease type id
T019; T047
mesh disease class id
C05; C16; C17
do disease class id
DOID:7; DOID:630
herb disease id
HBDIS002216
disgenet id
C0029434
mesh id
D010013
do id
110334; 110342; 110341; 110337;
icd10 id
Q78.0
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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_pinyinmatchingherbs.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