Relationship Graph Explorer
Follow the connections
Every herb, ingredient, formula, gene target, and disease — connected through real research. Search, pick a subject, and navigate the graph in any direction.
🌿
Herb
6,826
→
⚗️
Ingredient
44,595
→
🧬
Gene Target
15,505
→
🏥
Disease
30,170
→
🧪
Evidence
23,295
trials · metas · refs
Plus 6,743 TCM formulas connecting herbs together
74 Diseases matching "Hypogonadism"
Hypogonadism
Harding Ataxia
Hypopituitarism
Malouf Syndrome
Najjar Syndrome
Sheehan Syndrome
Kallmann Syndrome
Panhypopituitarism
Pituitary Cachexia
Pituitary Dwarfism
Kallmann Syndrome 1
Central Hypogonadism
Froehlich'S Syndrome
Primary Hypogonadism
Reifenstein Syndrome
Pituitary Short Stature
Testicular Hypogonadism
Male Pseudohermaphroditism
Female Hypogonadism Syndrome
Hypogonadotropic Hypogonadism
Cerebellar Ataxia, Early Onset
Deafness-Hypogonadism Syndrome
Kallmann Syndrome 2 (Disorder)
Isolated Gonadotropin Deficiency
Myoclonic Cerebellar Dyssynergia
Idiopathic Growth Hormone Deficiency
Acquired Hypogonadotropic Hypogonadism
Eunuchoidism, Familial Hypogonadotropic
Follicle Stimulating Hormone Deficiency
Hypogonadism, Isolated Hypogonadotropic
Isolated Lutropin Deficiency (Disorder)
Congenital Hypogonadotropic Hypogonadism
Idiopathic Hypogonadotropic Hypogonadism
Isolated Deficiency of Pituitary Hormone
Necrosis of Pituitary Gland (Postpartum)
Arhinia, Choanal Atresia, And Microphthalmia
Hypogonadotropic Hypogonadism 2 With Anosmia
Hypogonadotropic Hypogonadism 18 With Anosmia
Hypogonadotropic Hypogonadism 22 With Anosmia
Hypogonadotropic Hypogonadism 3 Without Anosmia
Hypogonadotropic Hypogonadism 8 Without Anosmia
Hypogonadotrophic Hypogonadism 5 Without Anosmia
Hypogonadotropic Hypogonadism 10 Without Anosmia
Hypogonadotropic Hypogonadism 20 Without Anosmia
Leukodystrophy, Dysmyelinating, With Oligodontia
Follicle-Stimulating Hormone Deficiency, Isolated
Cerebellar Ataxia And Hypogonadotropic Hypogonadis
Type I Familial Incomplete Male Pseudohermaphrodit
Hypogonadotropic Hypogonadism 3 With Or Without An
Hypogonadotropic Hypogonadism 4 With Or Without An
Hypogonadotropic Hypogonadism 5 With Or Without An
Hypogonadotropic Hypogonadism 6 With Or Without An
Hypogonadotropic Hypogonadism 8 With Or Without An
Hypogonadotropic Hypogonadism 9 With Or Without An
Hypogonadotropic Hypogonadism 10 With Or Without A
Hypogonadotropic Hypogonadism 11 With Or Without A
Hypogonadotropic Hypogonadism 13 With Or Without A
Hypogonadotropic Hypogonadism 14 With Or Without A
Hypogonadotropic Hypogonadism 15 With Or Without A
Hypogonadotropic Hypogonadism 16 With Or Without A
Hypogonadotropic Hypogonadism 17 With Or Without A
Hypogonadotropic Hypogonadism 18 With Or Without A
Hypogonadotropic Hypogonadism 19 With Or Without A
Hypogonadotropic Hypogonadism 20 With Or Without A
Hypogonadotropic Hypogonadism 21 With Or Without A
Hypogonadotropic Hypogonadism 22 With Or Without A
Hypogonadotropic Hypogonadism 18 With Anosmia, Sus
Hypogonadotropic Hypogonadism 21 With Anosmia, Sus
Mental Retardation, X-Linked, With Short Stature,
Chorioretinal Dystrophy, Spinocerebellar Ataxia, A
Leukodystrophy, Hypomyelinating, With Hypodontia A
Moyamoya Disease 4 With Short Stature, Hypergonado
Leukodystrophy, Hypomyelinating, 8, With Or Withou
Mental Retardation, Epileptic Seizures, Hypogonadi
🏥 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
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_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