DiseaseID 16449

糖原贮积症0型,肌肉型

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: 3Links: 4
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Record Fields

Scalar fields from the final disease record.

Disease Id
16449
Core Entity Id
74526
Source Entity Count
1
Preferred Name
Glycogen Storage Disease 0, Muscle
Name Cn
糖原贮积症0型,肌肉型
Name Pinyin
Tang Yuan Zhu Ji Zheng 0 Xing , Ji Rou Xing
Name En
Glycogen Storage Disease 0, Muscle
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
Version
v1
Suppressed
No

Names

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

Name
Glycogen Storage Disease 0, Muscle
Role
preferred
Name
GSD 0b
Role
alias
Name
MUSCLE GLYCOGEN STORAGE DISEASE 0
Role
alias
Name
MUSCLE GLYCOGEN SYNTHASE DEFICIENCY
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS018722
Omim
611556
Umls
C1969054
Sym Map
SMDE00843
Dis Ge Net
C1969054
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
26251

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
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