Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Formula: 5Herb: 1Target: 20Links: 30
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 7380
- Core Entity Id
- 64164
- Source Entity Count
- 1
- Preferred Name
- Leydig Cell Agenesis
- Name Cn
- 睾丸间质细胞发育不全
- Name Pinyin
- Gao Wan Jian Zhi Xi Bao Fa Yu Bu Quan
- Name En
- Leydig Cell Agenesis
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Male Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Leydig Cell Agenesis
Role
preferred
Name
Leydig Cell Hypoplasia, Type I
Role
preferred
Name
46,XY Disorder of Sex Development Due To LH Defects
Role
preferred
Name
Leydig Cell Hypoplasia
Role
preferred
Name
Leydig Cell Hypoplasia, Type II
Role
preferred
Name
Luteinizing Hormone Resistance, Female
Role
preferred
Name
HYPERGONADOTROPIC HYPOGONADISM, MALE, DUE TO LHCGR DEFECT
Role
alias
Name
LEYDIG CELL HYPOPLASIA WITH MALE PSEUDOHERMAPHRODITISM
Role
alias
Name
LEYDIG CELL HYPOPLASIA, COMPLETE
Role
alias
Name
LEYDIG CELL HYPOPLASIA, PARTIAL
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS005996HBDIS012157HBDIS019263HBDIS021987HBDIS022083
Omim
238320
Umls
C0266432C2673497C3668935
Sym Map
SMDE01567
Dis Ge Net
C0266432C0860158C2673497C3668935C3714042
Umls Sty
T019T047
Me Sh Class
C12C13C16C19
Etcm Disease
Leydig Cell Hypoplasia, Type I
Tcmbank Disease
106652508126706302506429
Itcmdb Generated
ITX-DISEASE-18E46AA80272ITX-DISEASE-DDCC407E1191
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Leydig Cell Hypoplasia, Type I Details page
Disease Type
disease
Umls Disease Type
Congenital AbnormalityDisease or Syndrome
Basic Information
Disease Name
Leydig Cell Hypoplasia, Type I
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Endocrine diseases;Reproductive diseases
Me Sh Disease Class
Male Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
Umls Semantic Type Name
Congenital AbnormalityDisease or Syndrome