DiseaseID 12445
先天性蔗糖酶-异麦芽糖酶缺乏症
disease
CSP2006:characterized by the deficiency or absence of the enzymes sucrase and isomaltase existing at, and usually before birth; this enzyme complex (sucrase-isomaltase) assists in the breakdown of a certain sugar (ie, su
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Disease: 1Symptom: 5Target: 1Links: 6
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 12445
- Core Entity Id
- 69956
- Source Entity Count
- 1
- Preferred Name
- Sucrase-Isomaltase Deficiency, Congenital
- Name Cn
- 先天性蔗糖酶-异麦芽糖酶缺乏症
- Name Pinyin
- Xian Tian Xing Zhe Tang Mei - Yi Mai Ya Tang Mei Que Fa Zheng
- Name En
- Sucrase-Isomaltase Deficiency, Congenital
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- CSP2006:characterized by the deficiency or absence of the enzymes sucrase and isomaltase existing at, and usually before birth; this enzyme complex (sucrase-isomaltase) assists in the breakdown of a certain sugar (ie, sucrose) and certain products of starch digestion (dextrins); only evident soon after birth when sucrose or starches, such as found in modified milk formulas with sucrose or polycose, are ingested by an affected infant, breast-fed infants or those on lactose-only formula manifest no symptoms until such time as sucrose (found in fruit juices, solid foods, and/or some medications) is introduced into the diet.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Sucrase-Isomaltase Deficiency, Congenital
Role
preferred
Name
CSID
Role
alias
Name
DISACCHARIDE INTOLERANCE I
Role
alias
Name
SI DEFICIENCY
Role
alias
Name
SUCROSE INTOLERANCE, CONGENITAL
Role
alias
Name
SUCROSE-ISOMALTOSE MALABSORPTION, CONGENITAL
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS013205
Omim
222900
Umls
C1283620
Icd10
E74.31
Sym Map
SMDE03372
Dis Ge Net
C1283620
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
20695
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disease Definition
CSP2006:characterized by the deficiency or absence of the enzymes sucrase and isomaltase existing at, and usually before birth; this enzyme complex (sucrase-isomaltase) assists in the breakdown of a certain sugar (ie, sucrose) and certain products of starch digestion (dextrins); only evident soon after birth when sucrose or starches, such as found in modified milk formulas with sucrose or polycose, are ingested by an affected infant, breast-fed infants or those on lactose-only formula manifest no symptoms until such time as sucrose (found in fruit juices, solid foods, and/or some medications) is introduced into the diet.
Me Sh Disease Class
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
Umls Semantic Type Name
Disease or Syndrome