Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 17Herb: 12Symptom: 2Target: 18Links: 55
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 14379
- Core Entity Id
- 72156
- Source Entity Count
- 1
- Preferred Name
- Iridogoniodysgenesis, Type 2
- Name Cn
- 虹膜角发育不良2型
- Name Pinyin
- Hong Mo Jiao Fa Yu Bu Liang 2 Xing
- Name En
- Iridogoniodysgenesis, Type 2
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Eye DiseasesEye Diseases; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesEye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
- Do Class
- genetic disease
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Stomatognathic DiseasesEye Diseases
- Hpo Class Name
- Do Class Name
- genetic disease
- Disease Definition
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Iridogoniodysgenesis, Type 2
Role
preferred
Name
Anterior Segment Dysgenesis 3
Role
preferred
Name
Iridogoniodysgenesis, Type 1 (Disorder)
Role
preferred
Name
IRIS HYPOPLASIA WITH GLAUCOMA
Role
preferred
Name
ASGD3
Role
alias
Name
Anterior Segment Dysgenesis 4
Role
alias
Name
GLAUCOMA IRIDOGONIODYSPLASIA, FAMILIAL
Role
alias
Name
IGDA
Role
alias
Name
IRID1
Role
alias
Name
IRIDOGONIODYSGENESIS ANOMALY, AUTOSOMAL DOMINANT
Role
alias
Name
IRIDOGONIODYSGENESIS, TYPE 1
Role
alias
Name
Iridogoniodysgenesis Syndrome
Role
alias
Name
Iridogoniodysgenesis Type 2
Role
alias
Name
Iridogoniodysgenesis, Dominant Type
Role
alias
Name
Iris Hypoplasia And Glaucoma
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS015810HBDIS015900HBDIS018322
Omim
137600601631
Umls
C1839928C1866560C1866561
Sym Map
SMDE00377SMDE10080
Do Class
DOID:630
Dis Ge Net
C1839928C1842031C1866560
Umls Sty
T047
Me Sh Class
C07C11C16
Etcm Disease
Anterior Segment Dysgenesis 3
Tcmbank Disease
257625839690
Itcmdb Generated
ITX-DISEASE-2007C8B50107ITX-DISEASE-35501D9C8B63
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Page Title
Disease Anterior Segment Dysgenesis 3 Details page
Do Class Name
genetic disease
Disease Type
disease
Do Disease Class
genetic disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Anterior Segment Dysgenesis 3
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases;Eye diseases
Me Sh Disease Class
Eye DiseasesEye Diseases; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesEye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Stomatognathic DiseasesEye Diseases
Umls Semantic Type Name
Disease or Syndrome