DiseaseID 2434

Mitchell-Riley综合征

disease

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Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

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Disease: 1Symptom: 1Target: 17Links: 25
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Record Fields

Scalar fields from the final disease record.

Disease Id
2434
Core Entity Id
2746
Source Entity Count
1
Preferred Name
Mitchell-Riley Syndrome
Name Cn
Mitchell-Riley综合征
Name Pinyin
Mitchell-riley Zong He Zheng
Name En
Mitchell-Riley Syndrome
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version
v1,v2
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Mitchell-Riley Syndrome
Role
preferred
Name
DIABETES, NEONATAL, WITH PANCREATIC HYPOPLASIA, INTESTINAL ATRESIA, AND GALLBLADDER APLASIA OR HYPOPLASIA
Role
alias
Name
MTCHRS
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS029169
Omim
615710
Umls
C2748662
Sym Map
SMDE01623
Dis Ge Net
C2748662
Umls Sty
T047
Me Sh Class
C06C16C18C19
Etcm Disease
Mitchell-Riley Syndrome
Itcmdb Generated
ITX-DISEASE-779E0B4FE43C

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Mitchell-Riley Syndrome Details page
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Mitchell-Riley Syndrome
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Endocrine diseases;Gastrointestinal Diseases;Liver diseases
Me Sh Disease Class
Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Endocrine System Diseases
Dis Ge Net Disease Type
disease