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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
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_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