DiseaseID 13355
少精症
disease
Male sterility due to chromosome Y deletion is characterized by a severe deficiency of spermatogenesis. Chromosome Y deletions are a frequent genetic cause of male infertility.
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Disease: 1Symptom: 2Target: 12Links: 14
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 13355
- Core Entity Id
- 70982
- Source Entity Count
- 2
- Preferred Name
- Oligospermia
- Name Cn
- 少精症
- Name Pinyin
- Shao Jing Zheng
- Name En
- Oligospermia
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Cell or Molecular Dysfunction
- Disgenet Type
- disease
- Mesh Class
- Female Urogenital Diseases and Pregnancy Complications; Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System DiseasesMale Urogenital DiseasesMale Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Abnormality of the genitourinary system
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital DiseasesMale Urogenital DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
- Hpo Class Name
- Abnormality of the genitourinary system
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- Male sterility due to chromosome Y deletion is characterized by a severe deficiency of spermatogenesis. Chromosome Y deletions are a frequent genetic cause of male infertility.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Oligospermia
Role
preferred
Name
Partial Chromosome Y Deletion
Role
preferred
Name
Male Sterility Due To Y-Chromosome Deletions
Role
preferred
Name
Sertoli Cell-Only Syndrome, Type 1
Role
preferred
Name
Spermatogenic Failure, Nonobstructive, Y-Linked
Role
preferred
Name
Hypospermatogenesis
Role
alias
Name
Low Sperm Count
Role
alias
Name
Male Sterility Due To Chromosome Y Deletion
Role
alias
Name
Partial Deletion of Chromosome Y
Role
alias
Name
Sertoli Cell-Only Syndrome, Type I
Role
alias
Name
Spermatogenic Failure, Y-Linked, 1
Role
alias
Name
Spermatogenic Failure, Y-Linked, 2
Role
alias
Name
Y-Linked Spermatogenic Failure 1
Role
alias
Name
Y-Linked Spermatogenic Failure 2
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
ETCM3215HBDIS002168HBDIS014321HBDIS015726HBDIS020236HBDIS027354
Umls
C1507149C2931163
Icd10
Q98.6
Sym Map
SMDE05102SMDE11597
Do Class
DOID:630DOID:7
Dis Ge Net
C0028960C1507149C1839071C2931163C4551960
Orphanet
1646
Umls Sty
T047T049
Hpo Class
HP:0000119
Me Sh Class
C12C13C16C19C23
Tcmbank Disease
1854619085200472984316905450
Itcmdb Generated
ITX-DISEASE-234D7F81F4A3ITX-DISEASE-454F1C1A3F12
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of the genitourinary system
Do Disease Class
disease of anatomical entity; genetic disease
Hpo Disease Class
Abnormality of the genitourinary system
Umls Disease Type
Cell or Molecular DysfunctionDisease or Syndrome
Disease Definition
Male sterility due to chromosome Y deletion is characterized by a severe deficiency of spermatogenesis. Chromosome Y deletions are a frequent genetic cause of male infertility.NCI2016_NICHD_1602D:Decreased number of spermatozoa in the semen.|NCI2016_CTCAE_1602D:A disorder characterized by a decrease in the number of spermatozoa in the semen.|NCI2016_02D:Decreased number of spermatozoa in the semen.|MSH2017_2016_08_12:A condition of suboptimal concentration of SPERMATOZOA in the ejaculated SEMEN to ensure successful FERTILIZATION of an OVUM. In humans, oligospermia is defined as a sperm count below 20 million per milliliter semen.|HPO2016_07_04:Reduced count of spermatozoa in the semen, defined as a sperm count below 20 million per milliliter semen. [HPO:probinson]
Me Sh Disease Class
Female Urogenital Diseases and Pregnancy Complications; Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System DiseasesMale Urogenital DiseasesMale Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital DiseasesMale Urogenital DiseasesPathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
Umls Semantic Type Name
Cell or Molecular DysfunctionDisease or Syndrome