Human Phenotype Ontology 
Grandparent Node:
expandAbnormal spermatogenesis (HP:0008669)help
Parent Node:
expandAzoospermia (HP:0000027)help
..Starting node
..expandPretesticular azoospermia (HP:0011963)help
Term ID: 11963
Name: Pretesticular azoospermia
Synonym:
Definition: Absence of any measurable level of sperm in his semen, due to a hypothalamic or pituitary abnormality diagnosed with hypo-gonadotropic-hypogonadism. The diagnosis is made on the basis of low LH and FSH levels and low or normal testosterone levels.
Comments:
Reference: HP:0011963
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandNon-obstructive azoospermia (HP:0011961) help
..expandObstructive azoospermia (HP:0011962) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011963HP:0011963Pretesticular azoospermia0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.