Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of prenatal development or birth (HP:0001197)help
Grandparent Node:
expandEdema (HP:0000969)help
Parent Node:
expandCystic hygroma (HP:0000476)help
Parent Node:
expandIncreased nuchal translucency (HP:0010880)help
..Starting node
..expandFetal cystic hygroma (HP:0010878)help
Term ID: 10878
Name: Fetal cystic hygroma
Synonym: Foetal cystic hygroma
Definition: The presence during the prenatal period of a cystic mass with multiple septa with multiple, asymmetric, thin-walled cysts near the posterior aspect of the neck. Fetal cystic hygroma can be defined as nuchal translucency with or without septations measuring greater than 3.0 mm. Increased NT refers to a measurement above the 95th centile, and the term is used irrespective of whether the collection of fluid is septated or not, and whether it is confined to the neck or envelopes the whole fetus. After 14 weeks, increased NT usually resolves, but in some cases it evolves into nuchal edema or cystic hygromas.
Comments:
Reference: HP:0010878
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010878HP:0010878Fetal cystic hygroma0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.