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): Mild microcephaly

(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)
+ + + + + + 6:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + 5:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + 4:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + 4:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ + + 3:   Abnormal skull morphology [HP:0000929] <14>(25|38) (28|22|20)
+ + 2:   Abnormality of skull size [HP:0000240] <2>(14|23) (15|11|5)
+ 1:   Decreased head circumference [HP:0040195] <2>(7|13) (8|5|1)
0:   Mild microcephaly [HP:0040196](0|0) (0|0|0)