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Phenotypic Abnormality (PA): Facial hemangioma

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Neoplasm [HP:0002664] <2>(20|21) (23|8|3)
+ + + + 4:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + + + 4:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + 3:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
+ + + 3:   Neoplasm by anatomical site [HP:0011793] <24>(18|19) (20|7|2)
+ + + 3:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + 2:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + 2:   Vascular neoplasm [HP:0100742] <2>(2|1) (2|0|0)
+ 1:   Hemangioma [HP:0001028] <24>(2|1) (2|0|0)
+ 1:   Abnormality of facial soft tissue [HP:0011799] <7>(2|3) (4|3|0)
0:   Facial hemangioma [HP:0000329] <3>(0|0) (0|0|0)
- 1:   Facial capillary hemangioma [HP:0000996] <3>(0|0) (0|0|0)
- 1:   Facial midline hemangioma [HP:0004664](0|0) (0|0|0)
- 1:   Plaque-like facial hemangioma [HP:0007434](0|0) (0|0|0)