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Phenotypic Abnormality (PA): Hypermelanotic macule

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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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|37|15)
+ + + + 4:   Abnormality of the skin [HP:0000951] <4>(34|55) (45|36|12)
+ + + 3:   Abnormality of skin morphology [HP:0011121] <22>(29|49) (40|31|11)
+ + + 3:   Abnormality of skin pigmentation [HP:0001000] <17>(2|8) (4|2|0)
+ + 2:   Localized skin lesion [HP:0011355] <29>(12|20) (18|10|6)
+ + 2:   Hyperpigmentation of the skin [HP:0000953] <6>(0|2) (0|0|0)
+ 1:   Macule [HP:0012733] <4>(0|1) (0|0|0)
+ 1:   Irregular hyperpigmentation [HP:0007400] <11>(0|1) (0|0|0)
0:   Hypermelanotic macule [HP:0001034] <4>(0|1) (0|0|0)
- 1:   Large cafe-au-lait macules with irregular margins [HP:0005605](0|0) (0|0|0)
- 1:   Macular hyperpigmented dermopathy [HP:0007412](0|0) (0|0|0)
- 1:   Mongolian blue spot [HP:0011369](0|0) (0|0|0)
- 1:   Multiple lentigines [HP:0001003](0|0) (0|0|0)