DiseaseID 4099

戊糖尿症

disease

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Disease: 1Symptom: 1Target: 9Links: 10
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Record Fields

Scalar fields from the final disease record.

Disease Id
4099
Core Entity Id
60395
Source Entity Count
1
Preferred Name
Pentosuria
Name Cn
戊糖尿症
Name Pinyin
Wu Tang Niao Zheng
Name En
Pentosuria
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 DiseasesFemale Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Do Class
disease of anatomical entitygenetic disease; disease of anatomical entity; disease of metabolism
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Hpo Class Name
Do Class Name
disease of anatomical entitydisease of metabolism; genetic disease; disease of anatomical entity
Disease Definition
Version
v2
Suppressed
No

Names

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

Name
Pentosuria
Role
preferred
Name
Familial Renal Glucosuria
Role
preferred
Name
Glycosuria, Renal
Role
preferred
Name
Renal Glucosuria
Role
alias
Name
Renal Glycosuria
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS001198HBDIS006204HBDIS020989
Me Sh
D006030
Omim
260800
Umls
C3245525
Sym Map
SMDE08651
Do Class
DOID:0014667DOID:630DOID:7
Dis Ge Net
C0017980C0268162C3245525
Umls Sty
T047
Me Sh Class
C12C13C16C18
Tcmbank Disease
17644217765066
Itcmdb Generated
ITX-DISEASE-9EF2E43EC71B

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Do Class Name
disease of anatomical entitydisease of metabolism; genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entitygenetic disease; disease of anatomical entity; disease of metabolism
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic DiseasesFemale Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; 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 DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Umls Semantic Type Name
Disease or Syndrome