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Phenotypic Abnormality (PA): Abnormality of the umbilical cord

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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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of prenatal development or birth [HP:0001197] <18>(10|15) (12|6|4)
+ 1:   Abnormalities of placenta or umbilical cord [HP:0001194] <4>(0|1) (1|2|1)
0:   Abnormality of the umbilical cord [HP:0010881] <11>(0|0) (0|0|0)
- 1:   Abnormal insertion of umbilical cord [HP:0011418] <3>(0|0) (0|0|0)
- 1:   Abnormal umbilical cord blood vessels [HP:0011403] <3>(0|0) (0|0|0)
- 1:   Abnormal cord blood measurement [HP:0410210] <1>(0|0) (0|0|0)
- 1:   Delayed umbilical cord separation [HP:0032434](0|0) (0|0|0)
- 1:   Long umbilical cord [HP:0011417](0|0) (0|0|0)
- 1:   Neonatal omphalitis [HP:0032435](0|0) (0|0|0)
- 1:   Short umbilical cord [HP:0001196](0|0) (0|0|0)
- 1:   Umbilical cord cyst [HP:0030654](0|0) (0|0|0)
- 1:   Umbilical cord hematoma [HP:0030657](0|0) (0|0|0)
- 1:   Umbilical cord knot [HP:0030655](0|0) (0|0|0)
- 1:   Umbilical vein varix [HP:0030656](0|0) (0|0|0)