SUPERFAMILY 1.75 HMM library and genome assignments server

SUPERFAMILY 2 can be accessed from supfam.org. Please contact us if you experience any problems.

Phenotypic Abnormality (PA): Spinal arteriovenous malformation

(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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + + 3:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + + 3:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
+ + + 3:   Abnormality of cardiovascular system morphology [HP:0030680] <3>(29|42) (31|19|20)
+ + 2:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
+ + 2:   Abnormal vascular morphology [HP:0025015] <12>(15|18) (16|11|10)
+ 1:   Abnormality of the spinal cord [HP:0002143] <16>(3|5) (3|0|2)
+ 1:   Arteriovenous malformation [HP:0100026] <8>(0|1) (0|0|0)
0:   Spinal arteriovenous malformation [HP:0002390](0|0) (0|0|0)