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🏥 Disease / Health Topic

Pachygyria

0
Clinical Trials
0
Meta-Analyses
0
PubMed References
🏥 All Disease / Health Topic data fields for Pachygyria
🏥 Names
Disease Name
Pachygyria
Alias Names
Syndromic X-Linked Intellectual Disability Najm Type; Pontocerebellar Hypoplasia Type 8; Complex Cortical Dysplasia With Other Brain Malformations 7; Pontocerebellar Hypoplasia Type 9; Cerebral Pachygyria; Cortical Dysplasia-Focal Epilepsy Syndrome; Lissencephaly; Pontocerebellar Hypoplasia Type 7; Pontocerebellar Hypoplasia Type 2D; Joubert Syndrome; Agyria; Hydranencephaly; Macrogyria; Short-Rib Thoracic Dysplasia 14 With Polydactyly; Complex Cortical Dysplasia With Other Brain Malformations 1
Topic Type
disease
🧬 Ontology Classifications
DisGeNET Type
disease
UMLS Type
Congenital Abnormality
MeSH Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
HPO Class
Abnormality of the nervous system
DO Class
physical disorder; disease of mental health; genetic disease; syndrome; disease of anatomical entity
🔗 External References
Disease Ontology
110096; 90137; 4626; 50777; 6027
DisGeNET
C0266483
🔍 Raw view — every non-empty column on this row (29 fields)
name
Pachygyria
alias name
Syndromic X-Linked Intellectual Disability Najm Type; Pontocerebellar Hypoplasia Type 8; Complex Cortical Dysplasia With Other Brain Malformations 7; Pontocerebellar Hypoplasia Type 9; Cerebral Pachygyria; Cortical Dysplasia-Focal Epilepsy Syndrome; Lissencephaly; Pontocerebellar Hypoplasia Type 7; Pontocerebellar Hypoplasia Type 2D; Joubert Syndrome; Agyria; Hydranencephaly; Macrogyria; Short-Rib Thoracic Dysplasia 14 With Polydactyly; Complex Cortical Dysplasia With Other Brain Malformations 1; Pachygyria
topic type
disease
disgenet disease type
disease
umls disease type
Congenital Abnormality
mesh disease class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
hpo disease class
Abnormality of the nervous system
do disease class
physical disorder; disease of mental health; genetic disease; syndrome; disease of anatomical entity
umls disease type id
T019
mesh disease class id
C16; C10
hpo disease class id
HP:0000707
do disease class id
DOID:0080015; DOID:150; DOID:225
herb disease id
HBDIS006009
disgenet id
C0266483
mesh id
D054082
hpo id
HP:0001302; HP:0007227
do id
110096; 90137; 4626; 50777; 6027
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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: ACTIVE — direct link via herb_ingredients
  • Ingredient ↔ Target: ACTIVE — direct link via ingredient_targets
  • Target ↔ Disease: ACTIVE — direct link via target_health_topics
  • Herb → Target → Disease (full chemical spine): ACTIVE — joins all three link tables