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43 Diseases matching "Parkinson Disease"
Parkinson Disease Parkinson Disease 10 Parkinson Disease 12 Parkinson Disease 17 Parkinson Disease 18 Parkinsonian Disorders Parkinsonism, Juvenile Atypical Parkinson Disease Parkinsonism, Experimental Sporadic Parkinson Disease Secondary Parkinson Disease Atherosclerotic Parkinsonism Parkinson Disease, Late-Onset Young Onset Parkinson Disease Familial Juvenile Parkinsonism Parkinson Disease 8 (Disorder) Ramsay Hunt Paralysis Syndrome Autosomal Dominant Parkinsonism Parkinson Disease 16 (Disorder) Autosomal Recessive Parkinsonism Parkinson Disease 20, Early-Onset Parkinson Disease 19B, Early-Onset Parkinson Disease, Familial, Type 1 Parkinson Disease, Postencephalitic Parkinson Disease 19A, Juvenile-Onset Parkinson Disease, Secondary Vascular Parkinson Disease 5, Autosomal Dominant Parkinson Disease 22, Autosomal Dominant Parkinson Disease 14, Autosomal Recessive Parkinson Disease, Mitochondrial (Disorder) Autosomal Dominant Juvenile Parkinson Disease Autosomal Dominant Late Onset Parkinson Disease Parkinson Disease 2, Autosomal Recessive Juvenile Parkinson Disease 1, Autosomal Dominant (Disorder) Parkinson Disease 6, Late-Onset, Susceptibility To Parkinson Disease 15, Autosomal Recessive (Disorde Parkinson Disease 6, Autosomal Recessive Early-Ons Parkinson Disease 7, Autosomal Recessive Early-Ons Parkinson Disease 23, Autosomal Recessive Early-On Parkinson Disease 11, Autosomal Dominant, Suscepti Parkinson Disease 13, Autosomal Dominant, Suscepti Parkinson Disease 4, Autosomal Dominant Lewy Body Mitochondrial Complex I Deficiency, Mitochondrial
🏥 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