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Phenotypic Abnormality (PA): Abnormality of the chin

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + 2:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ 1:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
0:   Abnormality of the chin [HP:0000306] <12>(0|0) (0|0|0)
- 1:   Abnormality of depressor labii inferioris [HP:3000029](0|0) (0|0|0)
- 1:   Abnormality of mentalis muscle [HP:3000007](0|0) (0|0|0)
- 1:   Broad chin [HP:0011822](0|0) (0|0|0)
- 1:   Chin with H-shaped crease [HP:0011824](0|0) (0|0|0)
- 1:   Chin with horizontal crease [HP:0011823](0|0) (0|0|0)
- 1:   Chin with vertical crease [HP:0400001](0|0) (0|0|0)
- 1:   Cleft of chin [HP:0011323](0|0) (0|0|0)
- 1:   Dimple chin [HP:0010751](0|0) (0|0|0)
- 1:   Mandibular prognathia [HP:0000303](0|0) (0|0|0)
- 1:   Pointed chin [HP:0000307](0|0) (0|0|0)
- 1:   Short chin [HP:0000331](0|0) (0|0|0)
- 1:   Tall chin [HP:0400000](0|0) (0|0|0)