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Phenotypic Abnormality (PA): Abnormal venous morphology

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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 the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + 2:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
+ + 2:   Abnormality of cardiovascular system morphology [HP:0030680] <3>(29|42) (31|19|20)
+ 1:   Abnormal vascular morphology [HP:0025015] <12>(15|18) (16|11|10)
0:   Abnormal venous morphology [HP:0002624] <9>(1|1) (1|0|0)
- 1:   Prominent superficial veins [HP:0001015] <4>(0|0) (0|0|0)
- 1:   Abnormal jugular vein morphology [HP:3000042] <2>(0|0) (0|0|0)
- 1:   Abnormal vena cava morphology [HP:0005345] <2>(0|0) (0|0|0)
- 1:   Venous insufficiency [HP:0005293] <1>(1|1) (1|0|0)
- 1:   Abnormal facial vein morphology [HP:3000043](0|0) (0|0|0)
- 1:   Abnormal inferior thyroid vein morphology [HP:3000059](0|0) (0|0|0)
- 1:   Arteriovenous fistulas of celiac and mesenteric vessels [HP:0002642](0|0) (0|0|0)
- 1:   Venous malformation [HP:0012721](0|0) (0|0|0)
- 1:   Venous stenosis [HP:0025491](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
FnI-like domain0.008481Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
VWC domain0.0008383Direct


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)
FnI-like domain0.005397Inherited


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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