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): Abnormality of mylohyoid muscle

(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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + 4:   Abnormality of the mouth [HP:0000153] <2>(37|57) (46|32|22)
+ + + 3:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + + 3:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + 3:   Abnormal oral morphology [HP:0031816] <6>(35|53) (44|30|21)
+ + 2:   Abnormal oral cavity morphology [HP:0000163] <14>(28|43) (36|21|15)
+ + 2:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + 2:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
+ + 2:   Abnormality of facial soft tissue [HP:0011799] <7>(2|3) (4|3|0)
+ 1:   Abnormal mouth floor morphology [HP:0410012] <1>(0|0) (0|0|0)
+ 1:   Abnormality of facial musculature [HP:0000301] <12>(2|3) (4|3|0)
+ 1:   Abnormality of the submandibular region [HP:0410013] <1>(0|0) (0|0|0)
0:   Abnormality of mylohyoid muscle [HP:3000008](0|0) (0|0|0)