DiseaseID 3195
婴儿肠绞痛
phenotype
NCI2016_02D:Paroxysms of discomfort characterized by abrupt onset and remission. This typically occurs when a hollow organ or supporting structure is obstructed.|MSH2017_2016_08_12:A clinical syndrome with intermittent a
Relationship Network
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Disease: 1Symptom: 5Target: 1Links: 6
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3195
- Core Entity Id
- 59369
- Source Entity Count
- 1
- Preferred Name
- Infantile Colic
- Name Cn
- 婴儿肠绞痛
- Name Pinyin
- Ying Er Chang Jiao Tong
- Name En
- Infantile Colic
- Name Latin
- Bilingual Status
- complete
- Disease Type
- phenotype
- Umls Disease Type
- Finding
- Disgenet Type
- phenotype
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- Hpo Class
- Constitutional symptom; Abnormality of the digestive system
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Hpo Class Name
- Abnormality of the digestive system; Constitutional symptom
- Do Class Name
- Disease Definition
- NCI2016_02D:Paroxysms of discomfort characterized by abrupt onset and remission. This typically occurs when a hollow organ or supporting structure is obstructed.|MSH2017_2016_08_12:A clinical syndrome with intermittent abdominal pain characterized by sudden onset and cessation that is commonly seen in infants. It is usually associated with obstruction of the INTESTINES; of the CYSTIC DUCT; or of the URINARY TRACT.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Infantile Colic
Role
preferred
Name
Abdominal Colic
Role
preferred
Name
Abdominal Cramps
Role
preferred
Name
Colic
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS000002HBDIS004744HBDIS006058
Sym Map
SMDE05270SMDE09833
Dis Ge Net
C0000729C0232488C0266836
Umls Sty
T033T184
Hpo Class
HP:0025031HP:0025142
Me Sh Class
C16
Tcmbank Disease
12378244188201
Itcmdb Generated
ITX-DISEASE-4B4A1C62E5B6
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
phenotype
Hpo Class Name
Abnormality of the digestive system; Constitutional symptom
Hpo Disease Class
Constitutional symptom; Abnormality of the digestive system
Umls Disease Type
FindingSign or Symptom
Disease Definition
NCI2016_02D:Paroxysms of discomfort characterized by abrupt onset and remission. This typically occurs when a hollow organ or supporting structure is obstructed.|MSH2017_2016_08_12:A clinical syndrome with intermittent abdominal pain characterized by sudden onset and cessation that is commonly seen in infants. It is usually associated with obstruction of the INTESTINES; of the CYSTIC DUCT; or of the URINARY TRACT.NCI2016_NICHD_1602D:Consistent pattern of crying in a healthy infant between 3 weeks and 3 months of age. Often defined as lasting 3 hours a day more than 3 days a week for at least 3 weeks in a row.|NCI2016_02D:Paroxysms of irritability, fussing or crying that starts and stops without obvious cause in an infant up to four months of age without failure to thrive. Episodes last three or more hours per day for at least three days per week for at least on week.(NICHD)
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
phenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Umls Semantic Type Name
FindingSign or Symptom