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Phenotypic Abnormality (PA): Monochromacy

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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 eye [HP:0000478] <2>(64|78) (69|38|28)
+ + + 3:   Abnormal eye physiology [HP:0012373] <17>(34|47) (37|22|20)
+ + 2:   Abnormality of vision [HP:0000504] <15>(4|16) (9|8|8)
+ 1:   Color vision defect [HP:0000551] <3>(2|2) (2|0|0)
0:   Monochromacy [HP:0007803] <2>(1|0) (1|0|0)
- 1:   Cone monochromacy [HP:0011517] <1>(0|0) (0|0|0)
- 1:   Achromatopsia [HP:0011516](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
cAMP-binding domain-like0.000003839Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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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)
cAMP-binding domain-like0.000001577Direct


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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