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Phenotypic Abnormality (PA): Abnormal carotid artery morphology

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

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 cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + + 3:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
+ + + 3:   Abnormality of cardiovascular system morphology [HP:0030680] <3>(29|42) (31|19|20)
+ + 2:   Abnormal vascular morphology [HP:0025015] <12>(15|18) (16|11|10)
+ 1:   Abnormal systemic arterial morphology [HP:0011004] <24>(8|11) (9|4|2)
0:   Abnormal carotid artery morphology [HP:0005344] <12>(0|1) (0|0|0)
- 1:   Abnormal common carotid artery morphology [HP:0430021] <3>(0|0) (0|0|0)
- 1:   Carotid artery dissection [HP:0012158] <3>(0|0) (0|0|0)
- 1:   Abnormal internal carotid artery morphology [HP:3000062] <2>(0|0) (0|0|0)
- 1:   Abnormality of external carotid artery [HP:3000041](0|0) (0|0|0)
- 1:   Anomalous branches of internal carotid artery [HP:0005314](0|0) (0|0|0)
- 1:   Carotid artery dilatation [HP:0012163](0|0) (0|0|0)
- 1:   Carotid artery occlusion [HP:0012474](0|0) (0|0|0)
- 1:   Carotid artery stenosis [HP:0100546](0|0) (0|0|0)
- 1:   Carotid artery tortuosity [HP:0005302](0|0) (0|0|0)
- 1:   Carotid cavernous fistula [HP:0031157](0|0) (0|0|0)
- 1:   Carotid paraganglioma [HP:0100635](0|0) (0|0|0)
- 1:   Increased carotid artery intimal medial thickness [HP:0012273](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)
RecA protein-like (ATPase-domain)0.0001025Direct


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