DiseaseID 31738

常染色体显性Robinow综合征

Autosomal Dominant Robinow Syndrome

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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: 1Target: 21Links: 24
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Record Fields

Scalar fields from the final disease record.

Disease Id
31738
Core Entity Id
191672
Source Entity Count
1
Preferred Name
Autosomal Dominant Robinow Syndrome
Name Cn
常染色体显性Robinow综合征
Name Pinyin
Chang Ran Se Ti Xian Xing Robinow Zong He Zheng
Name En
Autosomal Dominant Robinow Syndrome
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
Suppressed

Names

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

Name
Autosomal Dominant Robinow Syndrome
Role
preferred
Source
ETCM_v2
Preferred
Yes

Cross References

Trusted external identifiers retained for this final record.

Etcm Disease
Autosomal Dominant Robinow Syndrome
Itcmdb Generated
ITX-DISEASE-5AF5C7F484F9

Attributes

Merged source attributes and domain-specific metadata.

Page Title
Disease Autosomal Dominant Robinow Syndrome Details page
Basic Information
Disease Name
Autosomal Dominant Robinow Syndrome
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Bone diseases;Nephrological diseases;Reproductive diseases;Smell/Taste diseases