DiseaseID 7520

肌肉AMP脱氨酶缺乏症

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: 3Target: 2Links: 5
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Record Fields

Scalar fields from the final disease record.

Disease Id
7520
Core Entity Id
64322
Source Entity Count
1
Preferred Name
Muscle Amp Deaminase Deficiency
Name Cn
肌肉AMP脱氨酶缺乏症
Name Pinyin
Ji Rou Amp Tuo An Mei Que Fa Zheng
Name En
Muscle Amp Deaminase Deficiency
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
v2
Suppressed
No

Names

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

Name
Muscle Amp Deaminase Deficiency
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS006184
Umls
C0268123
Icd10
E79.2
Sym Map
SMDE11164
Dis Ge Net
C0268123
Umls Sty
T047
Me Sh Class
C16C18
Tcmbank Disease
24096
Itcmdb Generated
ITX-DISEASE-750E7432FABD

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
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