DiseaseID 17249

稀毛症伴复发性皮肤水疱

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: 1Formula: 5Herb: 1Target: 17Links: 30
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Record Fields

Scalar fields from the final disease record.

Disease Id
17249
Core Entity Id
75451
Source Entity Count
1
Preferred Name
Hypotrichosis And Recurrent Skin Vesicles
Name Cn
稀毛症伴复发性皮肤水疱
Name Pinyin
Xi Mao Zheng Ban Fu Fa Xing Pi Fu Shui Pao
Name En
Hypotrichosis And Recurrent Skin Vesicles
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome; Congenital Abnormality
Disgenet Type
disease
Mesh Class
Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms
Do Class
Hpo Class
Mesh Class Name
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Hpo Class Name
Do Class Name
Disease Definition
Version
Suppressed

Names

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

Name
Hypotrichosis And Recurrent Skin Vesicles
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS019918
Omim
613102
Dis Ge Net
C2751292
Umls Sty
T019T047
Me Sh Class
C17C23
Etcm Disease
Hypotrichosis and Recurrent Skin Vesicles
Tcmbank Disease
15261
Itcmdb Generated
ITX-DISEASE-A40BDB3DDD97

Attributes

Merged source attributes and domain-specific metadata.

Page Title
Disease Hypotrichosis and Recurrent Skin Vesicles Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome; Congenital Abnormality
Basic Information
Disease Name
Hypotrichosis and Recurrent Skin Vesicles
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Skin diseases
Me Sh Disease Class
Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
Umls Semantic Type Name
Disease or Syndrome; Congenital Abnormality