DiseaseID 8922

脱发性毛周角化病

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: 4Links: 8
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Record Fields

Scalar fields from the final disease record.

Disease Id
8922
Core Entity Id
65921
Source Entity Count
1
Preferred Name
Keratosis Pilaris Decalvans
Name Cn
脱发性毛周角化病
Name Pinyin
Tuo Fa Xing Mao Zhou Jiao Hua Bing
Name En
Keratosis Pilaris Decalvans
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Congenital Abnormality
Disgenet Type
disease
Mesh Class
Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Hpo Class Name
Do Class Name
Disease Definition
Version
v2
Suppressed
No

Names

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

Name
Keratosis Pilaris Decalvans
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS008121
Umls
C0343057
Sym Map
SMDE10197
Dis Ge Net
C0343057
Umls Sty
T019
Me Sh Class
C16C17
Tcmbank Disease
24263
Itcmdb Generated
ITX-DISEASE-617CCCF352D5

Attributes

Merged source attributes and domain-specific metadata.

Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Congenital Abnormality
Me Sh Disease Class
Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Umls Semantic Type Name
Congenital Abnormality