Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Herb: 3Symptom: 4Target: 24Links: 31
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 6644
- Core Entity Id
- 63326
- Source Entity Count
- 1
- Preferred Name
- Diarrhea 6
- Name Cn
- 腹泻6
- Name Pinyin
- Fu Xie 6
- Name En
- Diarrhea 6
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Nutritional and Metabolic Diseases; Digestive System Diseases; Musculoskeletal DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and SymptomsDigestive System Diseases; Nervous System Diseases; Pathological Conditions, Signs and SymptomsDigestive System Diseases; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic DiseasesPathological Conditions, Signs and Symptoms; Digestive System Diseases; Nervous System DiseasesPathological Conditions, Signs and Symptoms; Digestive System Diseases; Nutritional and Metabolic Diseases
- Hpo Class Name
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Diarrhea 6
Role
preferred
Name
Diarrhea 4, Malabsorptive, Congenital
Role
preferred
Name
Diarrhea 5, With Tufting Enteropathy, Congenital
Role
preferred
Name
Neonatal Diarrhea
Role
preferred
Name
Congenital Secretory Diarrhea, Sodium Type (Disorder)
Role
preferred
Name
DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE
Role
preferred
Name
DIARRHEA 7, PROTEIN-LOSING ENTEROPATHY TYPE
Role
preferred
Name
Microvillus Inclusion Disease
Role
preferred
Name
Noninfective Neonatal Diarrhea
Role
preferred
Name
CTE
Role
alias
Name
Congenital Diarrhea 5 With Tufting Enteropathy
Role
alias
Name
Congenital Diarrhea 6
Role
alias
Name
Congenital Diarrhea 7 With Exudative Enteropathy
Role
alias
Name
Congenital Malabsorptive Diarrhea 4
Role
alias
Name
Congenital Secretory Sodium Diarrhea 3
Role
alias
Name
Congenital Secretory Sodium Diarrhea 8
Role
alias
Name
DIAR4
Role
alias
Name
DIAR5
Role
alias
Name
DIAR6
Role
alias
Name
Diarrhea 2, With Microvillus Atrophy
Role
alias
Name
Diarrhea 3, Secretory Sodium, Congenital
Role
alias
Name
Diarrhea 3, Secretory Sodium, Congenital, With Or Without Other Congenital Anomalies
Role
alias
Name
Diarrhea 8, Secretory Sodium, Congenital
Role
alias
Name
ENTERIC ANENDOCRINOSIS
Role
alias
Name
ENTEROPATHY, CONGENITAL TUFTING
Role
alias
Name
INTESTINAL EPITHELIAL CELL DYSPLASIA
Role
alias
Name
Noninfective Neonatal Diarrhoea
Role
alias
Name
Sodium Diarrhea, Congenital
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS005010HBDIS006118HBDIS007901HBDIS009745HBDIS015364HBDIS019882HBDIS021745HBDIS023031HBDIS028079
Omim
251850270420610370613217614616615863616868618183
Umls
C0235840C1835888C2750737C3553270
Icd10
P78.3
Sym Map
SMDE01907SMDE01972SMDE05016SMDE11347
Do Class
DOID:630DOID:7
Dis Ge Net
C0235840C0267663C0341306C0495452C1835888C2750737C3553270C4014516C4748579
Umls Sty
T019T047
Me Sh Class
C05C06C10C16C18C23
Etcm Disease
Diarrhea 10, Protein-Losing Enteropathy TypeDiarrhea 4, Malabsorptive, CongenitalDiarrhea 5, with Tufting Enteropathy, CongenitalDiarrhea 6Diarrhea 7, Protein-Losing Enteropathy Type
Tcmbank Disease
115401285213821151601525516791169812015128381
Itcmdb Generated
ITX-DISEASE-401CABA8B48BITX-DISEASE-5B10A30B3ADBITX-DISEASE-6F5B2568ED78ITX-DISEASE-A9D38B48185CITX-DISEASE-D055E039FF83
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2v2
Suppress
0
Page Title
Disease Diarrhea 10, Protein-Losing Enteropathy Type Details pageDisease Diarrhea 4, Malabsorptive, Congenital Details pageDisease Diarrhea 5, with Tufting Enteropathy, Congenital Details pageDisease Diarrhea 6 Details pageDisease Diarrhea 7, Protein-Losing Enteropathy Type Details page
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Congenital AbnormalityDisease or Syndrome
Basic Information
Disease Name
Diarrhea 10, Protein-Losing Enteropathy Type
Global Category
Genetic diseases
Anatomical Category
Gastrointestinal Diseases;Nephrological diseases
Disease Name
Diarrhea 4, Malabsorptive, Congenital
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Gastrointestinal Diseases
Disease Name
Diarrhea 5, with Tufting Enteropathy, Congenital
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Gastrointestinal Diseases
Disease Name
Diarrhea 6
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Gastrointestinal Diseases;Oral diseases
Disease Name
Diarrhea 7, Protein-Losing Enteropathy Type
Global Category
Genetic diseases
Anatomical Category
Gastrointestinal Diseases;Nephrological diseases
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Nutritional and Metabolic Diseases; Digestive System Diseases; Musculoskeletal DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and SymptomsDigestive System Diseases; Nervous System Diseases; Pathological Conditions, Signs and SymptomsDigestive System Diseases; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Musculoskeletal Diseases; Nervous System DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic DiseasesPathological Conditions, Signs and Symptoms; Digestive System Diseases; Nervous System DiseasesPathological Conditions, Signs and Symptoms; Digestive System Diseases; Nutritional and Metabolic Diseases
Umls Semantic Type Name
Congenital AbnormalityDisease or Syndrome