DiseaseID 4211
脐疝
disease
MSH2017_2016_08_12:A HERNIA due to an imperfect closure or weakness of the umbilical ring. It appears as a skin-covered protrusion at the UMBILICUS during crying, coughing, or straining. The hernia generally consists of
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Disease: 1Symptom: 4Target: 12Links: 16
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4211
- Core Entity Id
- 60526
- Source Entity Count
- 1
- Preferred Name
- Umbilical Hernia
- Name Cn
- 脐疝
- Name Pinyin
- Qi Shan
- Name En
- Umbilical Hernia
- 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; Female Urogenital Diseases and Pregnancy Complications; Pathological Conditions, Signs and SymptomsCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms
- Do Class
- disease of anatomical entity; physical disorder
- Hpo Class
- Abnormality of connective tissue; Abnormality of the digestive system
- Mesh Class Name
- Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
- Hpo Class Name
- Abnormality of the digestive system; Abnormality of connective tissue
- Do Class Name
- disease of anatomical entity; physical disorder
- Disease Definition
- MSH2017_2016_08_12:A HERNIA due to an imperfect closure or weakness of the umbilical ring. It appears as a skin-covered protrusion at the UMBILICUS during crying, coughing, or straining. The hernia generally consists of OMENTUM or SMALL INTESTINE. The vast majority of umbilical hernias are congenital but can be acquired due to severe abdominal distention.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Umbilical Hernia
Role
preferred
Name
Congenital Exomphalos
Role
preferred
Name
Congenital Omphalocele
Role
preferred
Name
Exomphalos
Role
alias
Name
Hernia, Umbilical
Role
alias
Name
Omphalocele
Role
alias
Name
Omphalocoele
Role
alias
Name
Umbilical Hernias
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0001537HP:0001539
Herb
HBDIS001357HBDIS011610HBDIS013436
Me Sh
D006554
Umls
C0019322C1306503
Icd10
K42K42.9Q79.2
Sym Map
SMDE07454SMDE14078
Do Class
DOID:0080015DOID:7
Dis Ge Net
C0019322C0795690C1306503
Umls Sty
T019T047
Hpo Class
HP:0003549HP:0025031
Me Sh Class
C13C16C23
Tcmbank Disease
21495240123536
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity; physical disorder
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of the digestive system; Abnormality of connective tissue
Do Disease Class
disease of anatomical entity; physical disorder
Hpo Disease Class
Abnormality of connective tissue; Abnormality of the digestive system
Umls Disease Type
Congenital AbnormalityDisease or Syndrome
Disease Definition
MSH2017_2016_08_12:A HERNIA due to an imperfect closure or weakness of the umbilical ring. It appears as a skin-covered protrusion at the UMBILICUS during crying, coughing, or straining. The hernia generally consists of OMENTUM or SMALL INTESTINE. The vast majority of umbilical hernias are congenital but can be acquired due to severe abdominal distention.NCI2016_NICHD_1602D:Protrusion of the abdominal cavity contents through the abdominal wall at the umbilicus.|NCI2016_02D:Protrusion of the abdominal cavity contents through the abdominal wall at the umbilicus.|HPO2016_07_04:Protrusion of abdominal contents through a defect in the abdominal wall musculature around the umbilicus. Skin and subcutaneous tissue overlie the defect. [HPO:probinson]
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Pathological Conditions, Signs and SymptomsCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
Umls Semantic Type Name
Congenital AbnormalityDisease or Syndrome