Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Herb: 11Symptom: 1Target: 20Links: 36
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 13574
- Core Entity Id
- 71235
- Source Entity Count
- 1
- Preferred Name
- Meretoja Syndrome
- Name Cn
- 梅雷托亚综合征
- Name Pinyin
- Mei Lei Tuo Ya Zong He Zheng
- Name En
- Meretoja Syndrome
- 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; Nutritional and Metabolic Diseases
- Do Class
- genetic disease; disease of metabolism
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases
- Hpo Class Name
- Do Class Name
- disease of metabolism; genetic disease
- Disease Definition
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Meretoja Syndrome
Role
preferred
Name
Amyloidosis, Finnish Type
Role
preferred
Name
Lattice Corneal Dystrophy Type Ii
Role
preferred
Name
Cerebral Amyloid Angiopathy, Gsn-Related
Role
preferred
Name
AMYLOID CRANIAL NEUROPATHY WITH LATTICE CORNEAL DYSTROPHY
Role
alias
Name
AMYLOIDOSIS DUE TO MUTANT GELSOLIN
Role
alias
Name
AMYLOIDOSIS V
Role
alias
Name
AMYLOIDOSIS, MERETOJA TYPE
Role
alias
Name
CORNEAL DYSTROPHY, LATTICE TYPE II
Role
alias
Name
Finnish Type Amyloidosis
Role
alias
Name
LATTICE CORNEAL DYSTROPHY, TYPE II
Role
alias
Name
LCD2
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS014664HBDIS014674HBDIS019943
Omim
105120
Umls
C1622345C1628319C2751493
Sym Map
SMDE02712SMDE10339SMDE10912
Do Class
DOID:0014667DOID:630
Dis Ge Net
C1622345C1628319C2751493
Umls Sty
T047
Me Sh Class
C11C16C18
Etcm Disease
Amyloidosis, Finnish Type
Tcmbank Disease
115971667522056
Itcmdb Generated
ITX-DISEASE-0A2FC56D123DITX-DISEASE-67C3C6FDAE76
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Page Title
Disease Amyloidosis, Finnish Type Details page
Do Class Name
disease of metabolism; genetic disease
Disease Type
disease
Do Disease Class
genetic disease; disease of metabolism
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Amyloidosis, Finnish Type
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Bone diseases;Eye diseases;Nephrological diseases;Neuronal diseases;Skin diseases
Me Sh Disease Class
Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases
Umls Semantic Type Name
Disease or Syndrome