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Phenotypic Abnormality (PA): Abnormality of the testis size

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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

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)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of the genitourinary system [HP:0000119] <5>(73|72) (80|28|9)
+ + + + + 5:   Abnormality of the genital system [HP:0000078] <3>(35|34) (37|10|3)
+ + + + 4:   Abnormal reproductive system morphology [HP:0012243] <10>(28|27) (29|4|1)
+ + + 3:   Abnormal external genitalia [HP:0000811] <7>(15|11) (16|1|1)
+ + + 3:   Abnormality of the male genitalia [HP:0010461] <2>(14|11) (16|1|1)
+ + 2:   Abnormality of male external genitalia [HP:0000032] <9>(13|10) (15|1|1)
+ 1:   Abnormal testis morphology [HP:0000035] <21>(9|8) (10|0|1)
0:   Abnormality of the testis size [HP:0045058] <2>(0|1) (0|0|0)
- 1:   Aplasia/Hypoplasia of the testes [HP:0010468] <2>(0|1) (0|0|0)
- 1:   Macroorchidism [HP:0000053] <2>(0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
RecA protein-like (ATPase-domain)0.01312Inherited


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