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Phenotypic Abnormality (PA): Increased nuchal translucency

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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)
+ + + + 4:   Abnormality of metabolism/homeostasis [HP:0001939] <16>(75|82) (79|40|16)
+ + + 3:   Abnormal homeostasis [HP:0012337] <8>(44|47) (44|22|8)
+ + 2:   Abnormality of fluid regulation [HP:0011032] <2>(8|9) (7|2|1)
+ + 2:   Phenotypic abnormality [HP:0000118] <25>
+ 1:   Edema [HP:0000969] <25>(8|9) (7|2|1)
+ 1:   Abnormality of prenatal development or birth [HP:0001197] <18>(10|15) (12|6|4)
0:   Increased nuchal translucency [HP:0010880] <1>(0|0) (0|0|0)
- 1:   Fetal cystic hygroma [HP:0010878](0|0) (0|0|0)