DiseaseID 18381
瘦素受体缺陷
disease
NCI2016_02D:Deficiency or dysfunction of the leptin receptor associated with loss-of-function mutation(s) in the LEPR gene.
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 5Symptom: 2Target: 18Links: 31
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 18381
- Core Entity Id
- 76772
- Source Entity Count
- 1
- Preferred Name
- Leptin Receptor Deficiency
- Name Cn
- 瘦素受体缺陷
- Name Pinyin
- Shou Su Shou Ti Que Xian
- Name En
- Leptin Receptor Deficiency
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Do Class
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- Disease Definition
- NCI2016_02D:Deficiency or dysfunction of the leptin receptor associated with loss-of-function mutation(s) in the LEPR gene.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Leptin Receptor Deficiency
Role
preferred
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS021833
Omim
614963
Umls
C3554225
Sym Map
SMDE00137
Dis Ge Net
C3554225
Umls Sty
T047
Etcm Disease
Leptin Receptor Deficiency
Tcmbank Disease
20358
Itcmdb Generated
ITX-DISEASE-0EA9E5B7E11B
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Leptin Receptor Deficiency Details page
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Leptin Receptor Deficiency
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Endocrine diseases;Reproductive diseases
Disease Definition
NCI2016_02D:Deficiency or dysfunction of the leptin receptor associated with loss-of-function mutation(s) in the LEPR gene.
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome