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Phenotypic Abnormality (PA): Male hypogonadism

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the genitourinary system [HP:0000119] <5>(73|72) (80|28|9)
+ + + 3:   Abnormality of the endocrine system [HP:0000818] <16>(28|35) (35|13|5)
+ + + 3:   Abnormality of the genital system [HP:0000078] <3>(35|34) (37|10|3)
+ + 2:   Abnormal male reproductive system physiology [HP:0012874] <4>(2|3) (3|0|1)
+ + 2:   Puberty and gonadal disorders [HP:0008373] <13>(15|18) (20|3|1)
+ + 2:   Abnormality of reproductive system physiology [HP:0000080] <5>(9|9) (11|3|2)
+ 1:   Hypogonadism [HP:0000135] <4>(6|5) (7|3|1)
+ 1:   Functional abnormality of male internal genitalia [HP:0000025] <3>(2|3) (3|0|1)
0:   Male hypogonadism [HP:0000026](0|0) (0|0|0)