Relationship Graph Explorer

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Every herb, ingredient, formula, gene target, and disease — connected through real research. Search, pick a subject, and navigate the graph in any direction.

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Evidence

23,295

trials · metas · refs

Plus 6,743 TCM formulas connecting herbs together

28 Diseases matching "Myopia"

Myopia Mild Myopia Axial Myopia Index Myopia Severe Myopia Simple Myopia Moderate Myopia Myopia 1, X-Linked Deafness And Myopia Myopia 2 (Disorder) Myopia 3 (Disorder) Myopia 6 (Disorder) Myopia, Progressive Myopia, Degenerative Rare Isolated Myopia Myopia, Susceptibility To Obsolete Congenital Myopia Myopia 21, Autosomal Dominant Myopia 22, Autosomal Dominant Myopia 24, Autosomal Dominant Myopia 25, Autosomal Dominant Myopia 23, Autosomal Recessive Myopia 26, X-Linked, Female-Limited Joint Laxity, Short Stature, And Myopia Polydactyly, Postaxial, With Progressive Myopia Myopia, High, With Cataract And Vitreoretinal Dege Epiphyseal Dysplasia, Multiple, With Myopia And Co Hypertelorism, Severe, With Midface Prominence, My

🏥 Disease / Health Topic

Abetalipoproteinemia

Open on HERB 2.0 ↗

Clinical Trials

Meta-Analyses

PubMed References

🏥 All Disease / Health Topic data fields for Abetalipoproteinemia

🏥 Names

Disease Name

Abetalipoproteinemia

Alias Names

Tangier Disease; Hypolipoproteinemia; Norum Disease; Abetalipoproteinemia

Topic Type

syndrome

🧬 Ontology Classifications

DisGeNET Type

disease

UMLS Type

Disease or Syndrome

MeSH Class

Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

HPO Class

Abnormality of metabolism/homeostasis

DO Class

genetic disease; disease of metabolism

🔗 External References

HERB DB

MeSH

OMIM

HPO

Disease Ontology

1391; 1388; 1387; 1386

DisGeNET

C0000744

🔍 Raw view — every non-empty column on this row (30 fields)

name

Abetalipoproteinemia

alias name

Tangier Disease; Hypolipoproteinemia; Norum Disease; Abetalipoproteinemia

topic type

syndrome

disgenet disease type

disease

umls disease type

Disease or Syndrome

mesh disease class

Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

hpo disease class

Abnormality of metabolism/homeostasis

do disease class

genetic disease; disease of metabolism

umls disease type id

T047

mesh disease class id

C16; C18

hpo disease class id

HP:0001939

do disease class id

DOID:0014667; DOID:630

herb disease id

HBDIS000007

disgenet id

C0000744

mesh id

D000012

hpo id

HP:0008181

do id

1391; 1388; 1387; 1386

omim id

200100

No relationships found yet for this entity. Try picking one of the top-researched items above.

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: empty — needs HERB_herb_ingredient import
Ingredient ↔ Target: empty — needs HERB_ingredient_target import
Target ↔ Disease: empty — needs HERB_target_disease import
Herb → Target → Disease (full chemical spine): awaiting Phase 2e link tables