Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of prenatal development or birth (HP:0001197)help
Parent Node:
expandFetal ultrasound soft marker (HP:0011425)help
..Starting node
..expandEnlarged fetal cisterna magna (HP:0011427)help
Term ID: 11427
Name: Enlarged fetal cisterna magna
Synonym: Enlarged foetal cisterna magna
Definition: The cisterna magna is measured on a transaxial view of the fetal head angled 15 degrees caudal to the canthomeatal line. The anterior/posterior diameter is taken between the inferior/posterior surface of the vermis of the cerebellum to the inner surface of the cranium. An enlarged cisternal magna is defined by an anterior/posterior diameter of 10 mm or more (PMID:16100637).
Comments:
Reference: HP:0011427
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbsence of stomach bubble on fetal sonography (HP:0010963) help
..expandEchogenic fetal bowel (HP:0010943) help
..expandEchogenic intracardiac focus (HP:0010942) help
..expandFetal choroid plexus cysts (HP:0011426) help
..expandFetal fifth finger clinodactyly (HP:0011431) help
..expandFetal pyelectasis (HP:0010945) help
..expandHypoplasia of fetal nasal bone (HP:0011430) help
..expandMild fetal ventriculomegaly (HP:0010952) help
..expandShort fetal femur length (HP:0011428) help
..expandShort fetal humerus length (HP:0011429) help
..expandSingle umbilical artery (HP:0001195) help
..expandThickened nuchal skin fold (HP:0000474) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011427HP:0011427Enlarged fetal cisterna magna0 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.