DiseaseID 25821
角膜炎-鱼鳞病-耳聋综合征，常染色体显性
Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant
JABL99:OMIM differentiates the autosomal dominant (KID syndrome) from
Relationship Network
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Disease: 1Herb: 12Symptom: 10Target: 16Links: 46
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 25821
- Core Entity Id
- 118389
- Source Entity Count
- 1
- Preferred Name
- Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant
- Name Cn
- 角膜炎-鱼鳞病-耳聋综合征，常染色体显性
- Name Pinyin
- Jiao Mo Yan - Yu Lin Bing - Er Long Zong He Zheng ， Chang Ran Se Ti Xian Xing
- Name En
- Keratitis-Ichthyosis-Deafness Syndrome, 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
- JABL99:OMIM differentiates the autosomal dominant (KID syndrome) from
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C0265336
Sym Map
SMDE00467
Etcm Disease
Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant
Itcmdb Generated
ITX-DISEASE-269961F54988
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant Details page
Basic Information
Disease Name
Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Ear diseases;Eye diseases;Skin diseases
Disease Definition
JABL99:OMIM differentiates the autosomal dominant (KID syndrome) from