DiseaseID 18766

遗传性纤维化性皮肤异色病伴肌腱挛缩、肌病和肺纤维化

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: 5Target: 1Links: 6
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Record Fields

Scalar fields from the final disease record.

Disease Id
18766
Core Entity Id
77215
Source Entity Count
1
Preferred Name
Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis
Name Cn
遗传性纤维化性皮肤异色病伴肌腱挛缩、肌病和肺纤维化
Name Pinyin
Yi Chuan Xing Xian Wei Hua Xing Pi Fu Yi Se Bing Ban Ji Jian Luan Suo 、 Ji Bing He Fei Xian Wei Hua
Name En
Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version
v1,v2
Suppressed
No

Names

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

Name
Poikiloderma, Hereditary Fibrosing, With Tendon Contractures, Myopathy, And Pulmonary Fibrosis
Role
preferred
Name
POIKILODERMA, HEREDITARY SCLEROSING, WITH TENDON AND PULMONARY INVOLVEMENT
Role
alias
Name
POIKTMP
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS022426
Omim
615704
Umls
C3810325
Sym Map
SMDE03453
Dis Ge Net
C3810325
Umls Sty
T047
Tcmbank Disease
14160

Attributes

Merged source attributes and domain-specific metadata.

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