Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 20Herb: 3Symptom: 2Target: 18Links: 49
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 13871
- Core Entity Id
- 71575
- Source Entity Count
- 1
- Preferred Name
- Anophthalmia And Pulmonary Hypoplasia
- Name Cn
- 无眼畸形伴肺发育不全
- Name Pinyin
- Wu Yan Ji Xing Ban Fei Fa Yu Bu Quan
- Name En
- Anophthalmia And Pulmonary Hypoplasia
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
- Do Class
- genetic disease
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract 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
Anophthalmia And Pulmonary Hypoplasia
Role
preferred
Name
Microphthalmia, Isolated, With Coloboma 8
Role
preferred
Name
Microphthalmia, Syndromic 9
Role
preferred
Name
ANOPHTHALMIA, CLINICAL, WITH MILD FACIAL DYSMORPHISM AND VARIABLE MALFORMATIONS OF THE LUNG, HEART, AND DIAPHRAGM
Role
alias
Name
ANOPHTHALMIA/MICROPHTHALMIA AND PULMONARY HYPOPLASIA
Role
alias
Name
Anophthalmia With Pulmonary Hypoplasia
Role
alias
Name
MATTHEW-WOOD SYNDROME
Role
alias
Name
MCOPCB8
Role
alias
Name
MCOPS9
Role
alias
Name
PMD
Role
alias
Name
PULMONARY AGENESIS, MICROPHTHALMIA, AND DIAPHRAGMATIC DEFECT
Role
alias
Name
SPEAR SYNDROME
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS015102HBDIS021636
Omim
601186
Umls
C1832661C3540845
Sym Map
SMDE00482SMDE05930SMDE10981
Do Class
DOID:630
Dis Ge Net
C1832661C3540845
Umls Sty
T047
Me Sh Class
C08C11C16
Etcm Disease
Microphthalmia, Syndromic 9
Tcmbank Disease
2715427442
Itcmdb Generated
ITX-DISEASE-A82E0D159FA9ITX-DISEASE-B2EBDB255EBB
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Page Title
Disease Microphthalmia, Syndromic 9 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
Microphthalmia, Syndromic 9
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases;Ear diseases;Endocrine diseases;Eye diseases;Mental diseases;Neuronal diseases;Oral diseases;Reproductive diseases;Respiratory diseases
Me Sh Disease Class
Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases
Umls Semantic Type Name
Disease or Syndrome