DiseaseID 9392

血型缺失综合征

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: 2Target: 1Links: 3
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Record Fields

Scalar fields from the final disease record.

Disease Id
9392
Core Entity Id
66460
Source Entity Count
1
Preferred Name
Blood Group Deletion Syndrome
Name Cn
血型缺失综合征
Name Pinyin
Xue Xing Que Shi Zong He Zheng
Name En
Blood Group Deletion Syndrome
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; Nervous System Diseases
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System 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
Blood Group Deletion Syndrome
Role
preferred
Name
Mcleod Syndrome
Role
alias
Name
Neuroacanthocytosis, Mcleod Type
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS008784
Omim
300842
Sym Map
SMDE06499
Dis Ge Net
C0398568
Umls Sty
T047
Me Sh Class
C10C16
Tcmbank Disease
22411

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; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome