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Phenotypic Abnormality (PA): Abnormal distribution of retinal arterioles and venules

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + + + 4:   Abnormality of the eye [HP:0000478] <2>(64|78) (69|38|28)
+ + + + 4:   Abnormal posterior eye segment morphology [HP:0004329] <3>(16|11) (17|6|8)
+ + + 3:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ + + 3:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
+ + + 3:   Abnormal fundus morphology [HP:0001098] <10>(15|11) (16|6|8)
+ + 2:   Abnormal retinal morphology [HP:0000479] <27>(11|6) (12|5|8)
+ + 2:   Abnormality of the vasculature of the eye [HP:0008047] <4>(6|5) (6|4|1)
+ 1:   Abnormal retinal vascular morphology [HP:0008046] <15>(2|1) (2|2|1)
0:   Abnormal distribution of retinal arterioles and venules [HP:0007815](0|0) (0|0|0)