DiseaseID 26355
家族性进行性色素沉着伴或不伴色素减退
Hyperpigmentation With Or Without Hypopigmentation, Familial Progressive
SNOMEDCT_US_2016_09_01:Patches of hyperpigmentation in the skin, which are present at birth or in early infancy and increase in size and number with age. A rare autosomal dominant disorder.
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 7Herb: 4Target: 17Links: 35
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26355
- Core Entity Id
- 118923
- Source Entity Count
- 1
- Preferred Name
- Hyperpigmentation With Or Without Hypopigmentation, Familial Progressive
- Name Cn
- 家族性进行性色素沉着伴或不伴色素减退
- Name Pinyin
- Jia Zu Xing Jin Xing Xing Se Su Chen Zhuo Ban Huo Bu Ban Se Su Jian Tui
- Name En
- Hyperpigmentation With Or Without Hypopigmentation, Familial Progressive
- Name Latin
- Bilingual Status
- complete
- Disease Type
- Umls Disease Type
- Disgenet Type
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- SNOMEDCT_US_2016_09_01:Patches of hyperpigmentation in the skin, which are present at birth or in early infancy and increase in size and number with age. A rare autosomal dominant disorder.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hyperpigmentation With Or Without Hypopigmentation, Familial Progressive
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C1840392
Sym Map
SMDE03095
Etcm Disease
Hyperpigmentation with or Without Hypopigmentation, Familial Progressive
Itcmdb Generated
ITX-DISEASE-8DC4ECE62FB1
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Hyperpigmentation with or Without Hypopigmentation, Familial Progressive Details page
Basic Information
Disease Name
Hyperpigmentation with or Without Hypopigmentation, Familial Progressive
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Skin diseases
Disease Definition
SNOMEDCT_US_2016_09_01:Patches of hyperpigmentation in the skin, which are present at birth or in early infancy and increase in size and number with age. A rare autosomal dominant disorder.