SUPERFAMILY 1.75 HMM library and genome assignments server

Superfamily is undergoing a server migration - you are now browsing on the new server. Please contact us if you experience any problems.

Phenotypic Abnormality (PA): Renal hypoplasia

(show info)

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 urinary system [HP:0000079] <4>(38|41) (45|15|7)
+ + + + 4:   Abnormality of the upper urinary tract [HP:0010935] <2>(21|22) (22|7|3)
+ + + 3:   Abnormality of the kidney [HP:0000077] <3>(17|16) (18|6|3)
+ + 2:   Abnormal renal morphology [HP:0012210] <26>(14|11) (14|4|1)
+ 1:   Renal hypoplasia/aplasia [HP:0008678] <2>(1|1) (1|0|1)
0:   Renal hypoplasia [HP:0000089] <2>(0|0) (0|0|1)
- 1:   Bilateral renal hypoplasia [HP:0012584](0|0) (0|0|0)
- 1:   Unilateral renal hypoplasia [HP:0012583](0|0) (0|0|0)


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

Supra-domain (including individual superfamily)

(show details)
Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57196,57196,57184
  • 57196 - EGF/Laminin
  • 57196 - EGF/Laminin
  • 57184 - Growth factor receptor domain
  • 0.0007174Direct