DiseaseID 25826
Jawad综合征
Jawad Syndrome
JABL99:A craniodigital syndrome marked by characteristic facies, microcephaly, retrognathia, symmetrical digital defects, and retarded mental development.
Relationship Network
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Disease: 1Formula: 5Symptom: 2Target: 19Links: 31
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 25826
- Core Entity Id
- 118394
- Source Entity Count
- 1
- Preferred Name
- Jawad Syndrome
- Name Cn
- Jawad综合征
- Name Pinyin
- Jawad Zong He Zheng
- Name En
- Jawad Syndrome
- 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:A craniodigital syndrome marked by characteristic facies, microcephaly, retrognathia, symmetrical digital defects, and retarded mental development.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Jawad Syndrome
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C0796063
Sym Map
SMDE00490
Etcm Disease
Jawad Syndrome
Itcmdb Generated
ITX-DISEASE-A2D3417338DB
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Jawad Syndrome Details page
Basic Information
Disease Name
Jawad Syndrome
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Mental diseases;Neuronal diseases;Oral diseases
Disease Definition
JABL99:A craniodigital syndrome marked by characteristic facies, microcephaly, retrognathia, symmetrical digital defects, and retarded mental development.