ITCMDBv1
DiseaseID 3116

家族性高催乳素血症

disease

Familial hyperprolactinemia is a rare, genetic endocrine disorder characterized by persistently high prolactin serum levels (not associated with gestation, puerperium, drug intake or pituitary tumor)

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Disease: 1Symptom: 3Target: 1Links: 4
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Record Fields

Scalar fields from the final disease record.

Disease Id
3116
Core Entity Id
3525
Source Entity Count
1
Preferred Name
Familial Hyperprolactinemia
Name Cn
家族性高催乳素血症
Name Pinyin
Jia Zu Xing Gao Cui Ru Su Xue Zheng
Name En
Familial Hyperprolactinemia
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Nervous System Diseases; Endocrine System Diseases
Do Class
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Familial hyperprolactinemia is a rare, genetic endocrine disorder characterized by persistently high prolactin serum levels (not associated with gestation, puerperium, drug intake or pituitary tumor)
Version
v1
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Familial Hyperprolactinemia
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS030090
Sym Map
SMDE00478
Dis Ge Net
C4706551
Orphanet
397685
Umls Sty
T047
Me Sh Class
C10C19

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Umls Disease Type
Disease or Syndrome
Disease Definition
Familial hyperprolactinemia is a rare, genetic endocrine disorder characterized by persistently high prolactin serum levels (not associated with gestation, puerperium, drug intake or pituitary tumor)
Me Sh Disease Class
Nervous System Diseases; Endocrine System Diseases
Dis Ge Net Disease Type
disease