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.

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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
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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