DiseaseID 26346
3MC综合征2型
3Mc Syndrome 2
JABL99:A syndrome of blepharoptosis, strabismus, abdominal muscle defect, cryptorchidism, and developmental delay.
Relationship Network
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Disease: 1Formula: 5Symptom: 3Target: 18Links: 32
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 26346
- Core Entity Id
- 118914
- Source Entity Count
- 1
- Preferred Name
- 3Mc Syndrome 2
- Name Cn
- 3MC综合征2型
- Name Pinyin
- 3mc Zong He Zheng 2 Xing
- Name En
- 3Mc Syndrome 2
- 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 syndrome of blepharoptosis, strabismus, abdominal muscle defect, cryptorchidism, and developmental delay.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
3Mc Syndrome 2
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Umls
C0796279
Sym Map
SMDE03071
Etcm Disease
3mc Syndrome 2
Itcmdb Generated
ITX-DISEASE-2A1C64EE228F
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease 3mc Syndrome 2 Details page
Basic Information
Disease Name
3mc Syndrome 2
Global Category
Genetic diseases
Anatomical Category
Bone diseases;Eye diseases
Disease Definition
JABL99:A syndrome of blepharoptosis, strabismus, abdominal muscle defect, cryptorchidism, and developmental delay.