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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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Ingredient
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Gene Target
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Disease
30,170
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Evidence
23,295
trials · metas · refs
Plus 6,743 TCM formulas connecting herbs together
113 Diseases matching "Retinitis Pigmentosa"
Rp23 Gene
Usher Syndrome
Rod-Cone Dystrophy
Macular Degeneration
Retinitis Pigmentosa
Cone-Rod Dystrophy 15
Cone-Rod Dystrophy 16
Retinitis Pigmentosa 1
Retinitis Pigmentosa 3
Retinitis Pigmentosa 4
Retinitis Pigmentosa 7
Retinitis Pigmentosa 9
Retinitis Pigmentosa 10
Retinitis Pigmentosa 11
Retinitis Pigmentosa 13
Retinitis Pigmentosa 14
Retinitis Pigmentosa 17
Retinitis Pigmentosa 18
Retinitis Pigmentosa 19
Retinitis Pigmentosa 20
Retinitis Pigmentosa 25
Retinitis Pigmentosa 26
Retinitis Pigmentosa 27
Retinitis Pigmentosa 28
Retinitis Pigmentosa 30
Retinitis Pigmentosa 31
Retinitis Pigmentosa 35
Retinitis Pigmentosa 36
Retinitis Pigmentosa 42
Retinitis Pigmentosa 43
Retinitis Pigmentosa 44
Retinitis Pigmentosa 45
Retinitis Pigmentosa 46
Retinitis Pigmentosa 47
Retinitis Pigmentosa 48
Retinitis Pigmentosa 49
Retinitis Pigmentosa 51
Retinitis Pigmentosa 53
Retinitis Pigmentosa 54
Retinitis Pigmentosa 55
Retinitis Pigmentosa 56
Retinitis Pigmentosa 57
Retinitis Pigmentosa 58
Retinitis Pigmentosa 59
Retinitis Pigmentosa 60
Retinitis Pigmentosa 61
Retinitis Pigmentosa 62
Retinitis Pigmentosa 64
Retinitis Pigmentosa 65
Retinitis Pigmentosa 66
Retinitis Pigmentosa 67
Retinitis Pigmentosa 68
Retinitis Pigmentosa 69
Retinitis Pigmentosa 70
Retinitis Pigmentosa 71
Retinitis Pigmentosa 72
Retinitis Pigmentosa 73
Retinitis Pigmentosa 74
Retinitis Pigmentosa 75
Retinitis Pigmentosa 76
Retinitis Pigmentosa 77
Retinitis Pigmentosa 78
Retinitis Pigmentosa 79
Retinitis Pigmentosa 80
Retinitis Pigmentosa 81
Retinitis Pigmentosa 83
Retinitis Pigmentosa 84
Usher Syndrome, Type Iii
Hereditary Retinal Dystrophy
Leber Congenital Amaurosis 4
Pigmentary Retinal Dystrophy
Retinitis Pigmentosa Inversa
Leber Congenital Amaurosis 13
Leber Congenital Amaurosis 14
Leber Congenital Amaurosis 18
Sectoral Retinitis Pigmentosa
X-Linked Retinitis Pigmentosa
Retinitis Pigmentosa 7, Digenic
Retinitis Pigmentosa 2 (Disorder)
Retinitis Pigmentosa 12 (Disorder)
Retinitis Pigmentosa 29 (Disorder)
Retinitis Pigmentosa 33 (Disorder)
Retinitis Pigmentosa 37 (Disorder)
Retinitis Pigmentosa 38 (Disorder)
Retinitis Pigmentosa 39 (Disorder)
Retinitis Pigmentosa 40 (Disorder)
Retinitis Pigmentosa 41 (Disorder)
Autosomal Dominant Retinitis Pigmentosa
Leber Congenital Amaurosis 3 (Disorder)
Autosomal Recessive Retinitis Pigmentosa
Neuropathy Ataxia And Retinis Pigmentosa
Retinitis Pigmentosa 4, Autosomal Recessive
Retinitis Pigmentosa, Concentric (Disorder)
Cone-Rod Dystrophy, Aipl1-Related (Disorder)
Retinitis Pigmentosa, Juvenile, Lrat-Related
Retinitis Pigmentosa, Juvenile, Aipl1-Related
Retinitis Pigmentosa, Juvenile, Spata7-Related
Posterior Column Ataxia With Retinitis Pigmentosa
Retinitis Pigmentosa And Erythrocytic Microcytosis
Retinal Dystrophy, Early-Onset Severe, Lrat-Relate
Metaphyseal Chondrodysplasia With Retinitis Pigmen
Retinitis Pigmentosa 82 With Or Without Situs Inve
Intellectual Developmental Disorder And Retinitis
Retinal Degeneration, Autosomal Recessive, Clumped
Ataxia And Retinitis Pigmentosa With Isolated Vita
Cutis Verticis Gyrata, Retinitis Pigmentosa, And S
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pi
Short Stature, Hearing Loss, Retinitis Pigmentosa,
Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pi
Retinitis Pigmentosa, X-Linked, And Sinorespirator
Retinitis Pigmentosa, X-Linked, And Sinorespirator
Microphthalmia, Posterior, With Retinitis Pigmento
Hypoprebetalipoproteinemia, Acanthocytosis, Retini
🏥 Disease / Health Topic
Abetalipoproteinemia
0
Clinical Trials
0
Meta-Analyses
0
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
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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:
empty — needs
HERB_herb_ingredientimport - Ingredient ↔ Target:
empty — needs
HERB_ingredient_targetimport - Target ↔ Disease:
empty — needs
HERB_target_diseaseimport - Herb → Target → Disease (full chemical spine): awaiting Phase 2e link tables