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Phenotypic Abnormality (PA): Melanocytic nevus

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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:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|37|15)
+ + + 3:   Abnormality of the skin [HP:0000951] <4>(34|55) (45|36|12)
+ + 2:   Abnormality of skin morphology [HP:0011121] <22>(29|49) (40|31|11)
+ + 2:   Localized skin lesion [HP:0011355] <29>(12|20) (18|10|6)
+ 1:   Nevus [HP:0003764] <12>(0|2) (1|0|0)
+ 1:   Abnormality of skin pigmentation [HP:0001000] <17>(2|8) (4|2|0)
0:   Melanocytic nevus [HP:0000995] <4>(0|1) (0|0|0)
- 1:   Congenital giant melanocytic nevus [HP:0005600](0|0) (0|0|0)
- 1:   Hyperpigmented nevi [HP:0007481](0|0) (0|0|0)
- 1:   Hyperpigmented nevi and streak [HP:0005606](0|0) (0|0|0)
- 1:   Numerous congenital melanocytic nevi [HP:0005603](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Ras-binding domain, RBD0.00001526Direct


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