DiseaseID 26232

常染色体显性遗传精神发育迟滞2型

Mental Retardation, Autosomal Dominant 2

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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
26232
Core Entity Id
118800
Source Entity Count
1
Preferred Name
Mental Retardation, Autosomal Dominant 2
Name Cn
常染色体显性遗传精神发育迟滞2型
Name Pinyin
Chang Ran Se Ti Xian Xing Yi Chuan Jing Shen Fa Yu Chi Zhi 2 Xing
Name En
Mental Retardation, Autosomal Dominant 2
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disgenet Type
Mesh Class
Do Class
Hpo Class
Mesh Class Name
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
Mental Retardation, Autosomal Dominant 2
Role
preferred
Name
MRD2
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Omim
614113
Umls
C3279842
Sym Map
SMDE02523
Itcmdb Generated
ITX-DISEASE-D0A3C5E57AFB

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0