DiseaseID 18393

常染色体显性精神发育迟滞19型

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: 4Target: 1Links: 5
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Record Fields

Scalar fields from the final disease record.

Disease Id
18393
Core Entity Id
76785
Source Entity Count
1
Preferred Name
Mental Retardation, Autosomal Dominant 19
Name Cn
常染色体显性精神发育迟滞19型
Name Pinyin
Chang Ran Se Ti Xian Xing Jing Shen Fa Yu Chi Zhi 19 Xing
Name En
Mental Retardation, Autosomal Dominant 19
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
disease of mental health; genetic disease
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
genetic disease; disease of mental health
Disease Definition
Version
v1,v2
Suppressed
No

Names

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

Name
Mental Retardation, Autosomal Dominant 19
Role
preferred
Name
Autosomal Dominant Non-Syndromic Intellectual Disability 19
Role
alias
Name
MRD19
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS021858
Omim
615075
Umls
C3554449
Sym Map
SMDE04389
Do Class
DOID:150DOID:630
Dis Ge Net
C3554449
Umls Sty
T047
Tcmbank Disease
23301

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
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
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome