DiseaseID 26517
疣状肢端角化病
Acrokeratosis Verruciformis
NCI2016_02D:A rare genetic skin keratinization disorder with an autosomal dominant mode of inheritance. It is characterized by numerous flesh-colored warty papules on the back of the hands, medial aspect of the feet, kne
Relationship Network
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Disease: 1Formula: 15Herb: 12Target: 18Links: 51
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26517
- Core Entity Id
- 119085
- Source Entity Count
- 1
- Preferred Name
- Acrokeratosis Verruciformis
- Name Cn
- 疣状肢端角化病
- Name Pinyin
- You Zhuang Zhi Duan Jiao Hua Bing
- Name En
- Acrokeratosis Verruciformis
- 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
- NCI2016_02D:A rare genetic skin keratinization disorder with an autosomal dominant mode of inheritance. It is characterized by numerous flesh-colored warty papules on the back of the hands, medial aspect of the feet, knees, and elbows.|MSH2017_2016_08_12:An alleleic variant of Darier's disease.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Acrokeratosis Verruciformis
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C0265971
Sym Map
SMDE03870
Etcm Disease
Acrokeratosis Verruciformis
Itcmdb Generated
ITX-DISEASE-B9AD07B31163
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Acrokeratosis Verruciformis Details page
Basic Information
Disease Name
Acrokeratosis Verruciformis
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Skin diseases
Disease Definition
NCI2016_02D:A rare genetic skin keratinization disorder with an autosomal dominant mode of inheritance. It is characterized by numerous flesh-colored warty papules on the back of the hands, medial aspect of the feet, knees, and elbows.|MSH2017_2016_08_12:An alleleic variant of Darier's disease.