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🏥 Disease / Health Topic

Achondroplasia

0
Clinical Trials
0
Meta-Analyses
0
PubMed References
🏥 All Disease / Health Topic data fields for Achondroplasia
🏥 Names
Disease Name
Achondroplasia
Alias Names
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans; Achondroplasia; Saddan; Hypochondroplasia
Topic Type
disease
🧬 Ontology Classifications
DisGeNET Type
disease
UMLS Type
Congenital Abnormality
MeSH Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
DO Class
disease of anatomical entity; genetic disease
🔗 External References
ICD-10
Disease Ontology
4480; 111158; 80041
DisGeNET
C0001080
🔍 Raw view — every non-empty column on this row (28 fields)
name
Achondroplasia
alias name
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans; Achondroplasia; Saddan; Hypochondroplasia
topic type
disease
disgenet disease type
disease
umls disease type
Congenital Abnormality
mesh disease class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
do disease class
disease of anatomical entity; genetic disease
umls disease type id
T019
mesh disease class id
C05; C16
do disease class id
DOID:7; DOID:630
herb disease id
HBDIS000024
disgenet id
C0001080
mesh id
D000130
do id
4480; 111158; 80041
icd10 id
Q77.4
omim id
100800
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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