DiseaseID 26130
先天性耳聋伴甲营养不良，常染色体显性
Deafness, Congenital, With Onychodystrophy, Autosomal Dominant
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Target: 17Links: 24
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26130
- Core Entity Id
- 118698
- Source Entity Count
- 1
- Preferred Name
- Deafness, Congenital, With Onychodystrophy, Autosomal Dominant
- Name Cn
- 先天性耳聋伴甲营养不良，常染色体显性
- Name Pinyin
- Xian Tian Xing Er Long Ban Jia Ying Yang Bu Liang ， Chang Ran Se Ti Xian Xing
- Name En
- Deafness, Congenital, With Onychodystrophy, Autosomal Dominant
- 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
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Deafness, Congenital, With Onychodystrophy, Autosomal Dominant
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C2675730
Sym Map
SMDE02055
Etcm Disease
Deafness, Congenital, with Onychodystrophy, Autosomal Dominant
Itcmdb Generated
ITX-DISEASE-2E2A808DD3B4
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Deafness, Congenital, with Onychodystrophy, Autosomal Dominant Details page
Basic Information
Disease Name
Deafness, Congenital, with Onychodystrophy, Autosomal Dominant
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Ear diseases;Eye diseases;Neuronal diseases;Oral diseases;Skin diseases