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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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Herb
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Ingredient
44,595
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Gene Target
15,505
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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
Subject Type: 🌿 Herbs ⚗️ Ingredients 📜 Formulas 🧬 Targets 🏥 Diseases
Quick picks: Abetalipoproteinemia Abortion, Habitual Agenesis Acanthamoeba Keratitis Acanthosis Nigricans Achondrogenesis Achondroplasia Acne Vulgaris Acne Keloid Apert Syndrome
🏥 Disease / Health Topic

Apert Syndrome

Open on HERB 2.0 ↗
0
Clinical Trials
0
Meta-Analyses
0
PubMed References
🏥 All Disease / Health Topic data fields for Apert Syndrome
🏥 Names
Disease Name
Apert Syndrome
Alias Names
Sakati-Nyhan Syndrome; Apert Syndrome; Orofaciodigital Syndrome X; Syndrome, Apert; Warburg Micro Syndrome 4; Goldenhar Syndrome; Fraser Syndrome; Warburg Micro Syndrome 1; Warburg Micro Syndrome 2; Branchiootic Syndrome; Orofaciodigital Syndrome I; Pfeiffer Syndrome; Baraitser-Winter Syndrome; Acrocephalosyndactylia; Apert-Crouzon Disease; Weissenbacher-Zweymuller Syndrome; Warburg Micro Syndrome 3; Saethre-Chotzen Syndrome; Mobius Syndrome
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; syndrome
🔗 External References
HERB DB
HBDIS000033 ↗
MeSH
D000168 ↗
OMIM
101200 ↗
Disease Ontology
12960; 60359; 60229; 13501; 6023
DisGeNET
C0001193
🔍 Raw view — every non-empty column on this row (27 fields)
name
Apert Syndrome
alias name
Sakati-Nyhan Syndrome; Apert Syndrome; Orofaciodigital Syndrome X; Syndrome, Apert; Warburg Micro Syndrome 4; Goldenhar Syndrome; Fraser Syndrome; Warburg Micro Syndrome 1; Warburg Micro Syndrome 2; Branchiootic Syndrome; Orofaciodigital Syndrome I; Pfeiffer Syndrome; Baraitser-Winter Syndrome; Acrocephalosyndactylia; Apert-Crouzon Disease; Weissenbacher-Zweymuller Syndrome; Warburg Micro Syndrome 3; Saethre-Chotzen Syndrome; Mobius Syndrome
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; syndrome
umls disease type id
T019
mesh disease class id
C05; C16
do disease class id
DOID:7; DOID:225; DOID:630
herb disease id
HBDIS000033
disgenet id
C0001193
mesh id
D000168
do id
12960; 60359; 60229; 13501; 6023
omim id
101200
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_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