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
..expandShort fetal humerus length (HP:0011429)help
Term ID: 11429
Name: Short fetal humerus length
Synonym: Short fetal long bone in upper arm length; Short foetal humerus length; Short foetal long bone in upper arm length
Definition: A short humerus length is defined as a length below the 2.5th percentile for gestational age or as a measurement less than 0.9 of that predicted by the measured biparietal diameter. The humerus should be measured with the bone perpendicular to the ultrasound beam and with epiphyseal cartilages visible but not included in the measurement (PMID:16100637).
Comments:
Reference: HP:0011429
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
..expandEnlarged fetal cisterna magna (HP:0011427) 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
..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:0011429HP:0011429Short fetal humerus length0 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.