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Phenotypic Abnormality (PA): 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)
+ 1:   Localized skin lesion [HP:0011355] <29>(12|20) (18|10|6)
0:   Nevus [HP:0003764] <12>(0|2) (1|0|0)
- 1:   Melanocytic nevus [HP:0000995] <4>(0|1) (0|0|0)
- 1:   Nevus flammeus [HP:0001052] <3>(0|0) (0|0|0)
- 1:   Epidermal nevus [HP:0010816] <2>(0|1) (1|0|0)
- 1:   Connective tissue nevi [HP:0100898] <1>(0|0) (0|0|0)
- 1:   Atypical nevi in non-sun exposed areas [HP:0001074](0|0) (0|0|0)
- 1:   Atypical nevus [HP:0001062](0|0) (0|0|0)
- 1:   Blue nevus [HP:0100814](0|0) (0|0|0)
- 1:   Congenital panfollicular nevus [HP:0025471](0|0) (0|0|0)
- 1:   Nevus of Ota [HP:0009920](0|0) (0|0|0)
- 1:   Nevus sebaceus [HP:0025511](0|0) (0|0|0)
- 1:   Nevus spilus [HP:0025510](0|0) (0|0|0)
- 1:   Numerous nevi [HP:0001054](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Ras-binding domain, RBD0.0001843Direct
G proteins0.008367Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
P-loop containing nucleoside triphosphate hydrolases0.2281Inherited


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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