DiseaseID 18387

常染色体显性遗传智力障碍17型

disease

Back to Browse

Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

Click a node to open it in a new tab
Disease: 1Target: 1Links: 1
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
18387
Core Entity Id
76778
Source Entity Count
1
Preferred Name
Mental Retardation, Autosomal Dominant 17
Name Cn
常染色体显性遗传智力障碍17型
Name Pinyin
Chang Ran Se Ti Xian Xing Yi Chuan Zhi Li Zhang Ai 17 Xing
Name En
Mental Retardation, Autosomal Dominant 17
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Pathological Conditions, Signs and Symptoms
Do Class
disease of mental health; genetic disease
Hpo Class
Mesh Class Name
Pathological Conditions, Signs and Symptoms
Hpo Class Name
Do Class Name
genetic disease; disease of mental health
Disease Definition
Version
Suppressed

Names

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

Name
Mental Retardation, Autosomal Dominant 17
Role
preferred
Name
Schuurs-Hoeijmakers Syndrome
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021843
Omim
615009
Do Class
DOID:150DOID:630
Dis Ge Net
C3554343
Umls Sty
T047
Me Sh Class
C23
Tcmbank Disease
14148

Attributes

Merged source attributes and domain-specific metadata.

Do Class Name
genetic disease; disease of mental health
Disease Type
disease
Do Disease Class
disease of mental health; genetic disease
Umls Disease Type
Disease or Syndrome
Me Sh Disease Class
Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms
Umls Semantic Type Name
Disease or Syndrome