DiseaseID 12338

葡萄酒色斑伴眼皮肤黑变病

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: 1Symptom: 1Target: 3Links: 4
Arranging relationship network...

Record Fields

Scalar fields from the final disease record.

Disease Id
12338
Core Entity Id
69835
Source Entity Count
1
Preferred Name
Port-Wine Stain With Oculocutaneous Melanosis
Name Cn
葡萄酒色斑伴眼皮肤黑变病
Name Pinyin
Pu Tao Jiu Se Ban Ban Yan Pi Fu Hei Bian Bing
Name En
Port-Wine Stain With Oculocutaneous Melanosis
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; Nervous System Diseases
Do Class
Hpo Class
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Nervous System 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
Port-Wine Stain With Oculocutaneous Melanosis
Role
preferred
Name
Phacomatosis Pigmentovascularis
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS013076
Umls
C1274879
Sym Map
SMDE12325
Dis Ge Net
C1274879
Umls Sty
T019
Me Sh Class
C10C16C17
Tcmbank Disease
16698

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