DiseaseID 32445
AKT2突变所致家族性部分性脂肪营养不良
Familial Partial Lipodystrophy Due to Akt2 Mutations
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Herb: 2Target: 18Links: 26
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 32445
- Core Entity Id
- 192379
- Source Entity Count
- 1
- Preferred Name
- Familial Partial Lipodystrophy Due to Akt2 Mutations
- Name Cn
- AKT2突变所致家族性部分性脂肪营养不良
- Name Pinyin
- Akt2 Tu Bian Suo Zhi Jia Zu Xing Bu Fen Xing Zhi Fang Ying Yang Bu Liang
- Name En
- Familial Partial Lipodystrophy Due to Akt2 Mutations
- 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
- Suppressed
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Familial Partial Lipodystrophy Due to Akt2 Mutations
Role
preferred
Source
ETCM_v2
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Etcm Disease
Familial Partial Lipodystrophy Due to Akt2 Mutations
Itcmdb Generated
ITX-DISEASE-835AE30A251C
Attributes
Merged source attributes and domain-specific metadata.
Page Title
Disease Familial Partial Lipodystrophy Due to Akt2 Mutations Details page
Basic Information
Disease Name
Familial Partial Lipodystrophy Due to Akt2 Mutations
Global Category
Fetal diseases;Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Blood diseases;Cardiovascular diseases;Endocrine diseases;Liver diseases;Muscle diseases;Neuronal diseases;Skin diseases