DiseaseID 6115
羊水过少序列征
disease
NCI2016_02D:A congenital abnormality characterized by the absence of one or both kidneys.|HPO2016_07_04:Agenesis, that is, failure of the kidney to develop during embryogenesis and development. [HPO:probinson]
Relationship Network
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Disease: 1Symptom: 1Target: 12Links: 13
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 6115
- Core Entity Id
- 62720
- Source Entity Count
- 1
- Preferred Name
- Oligohydramnios Sequence
- Name Cn
- 羊水过少序列征
- Name Pinyin
- Yang Shui Guo Shao Xu Lie Zheng
- Name En
- Oligohydramnios Sequence
- 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 ComplicationsMale Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Pathological Conditions, Signs and Symptoms
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of the genitourinary system
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital DiseasesPathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
- Hpo Class Name
- Abnormality of the genitourinary system
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_02D:A congenital abnormality characterized by the absence of one or both kidneys.|HPO2016_07_04:Agenesis, that is, failure of the kidney to develop during embryogenesis and development. [HPO:probinson]
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Oligohydramnios Sequence
Role
preferred
Name
Congenital Absence Of Kidney
Role
preferred
Name
Congenital Absence of Kidneys Syndrome
Role
preferred
Name
Absent Kidney
Role
alias
Name
Bilateral Renal Agenesis
Role
alias
Name
Bilateral Renal Aplasia
Role
alias
Name
Hereditary Renal Agenesis
Role
alias
Name
Missing Kidney
Role
alias
Name
Potter'S Syndrome
Role
alias
Name
Renal Agenesis
Role
alias
Name
Renal Agenesis, Bilateral
Role
alias
Name
Renal Agenesis, Unspecified
Role
alias
Name
Renal Aplasia
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0010958
Herb
HBDIS004205HBDIS010016HBDIS014630
Icd10
Q60.1Q60.6
Sym Map
SMDE07428
Do Class
DOID:7
Dis Ge Net
C0178426C0542519C1609433
Umls Sty
T019T047
Hpo Class
HP:0000119
Me Sh Class
C12C13C16C23
Tcmbank Disease
10201826026289
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of the genitourinary system
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of the genitourinary system
Umls Disease Type
Congenital AbnormalityDisease or Syndrome
Disease Definition
NCI2016_02D:A congenital abnormality characterized by the absence of one or both kidneys.|HPO2016_07_04:Agenesis, that is, failure of the kidney to develop during embryogenesis and development. [HPO:probinson]
Me Sh Disease Class
Male Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy ComplicationsMale Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Pathological Conditions, Signs and Symptoms
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 DiseasesPathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Umls Semantic Type Name
Congenital AbnormalityDisease or Syndrome