Human Phenotype Ontology 
Grandparent Node:
expand
Abnormal axial skeleton morphology (HP:0009121)help
Parent Node:
expand
Abdominal wall defect (HP:0010866)help
Parent Node:
expand
Abnormal thorax morphology (HP:0000765)help
..Starting node
..expand
Thoracoabdominal wall defect (HP:0100656)help
Term ID: 100656
Name: Thoracoabdominal wall defect
Synonym: Thoracoabdominal schisis
Definition: Failure to close of the chest and abdominal wall likely caused by the failure of the ventral wall to close during week 4 of development.
Comments:
Reference: HP:0100656
Genes and Diseases:
 
       Child Nodes:
........expandThoracoabdominal eventration (HP:0100657) help

 Sister Nodes: 
..expandAbnormal clavicle morphology (HP:0000889) help
..expandAbnormal rib cage morphology (HP:0001547) help
..expandAbnormal scapula morphology (HP:0000782) help
..expandAbnormal shoulder morphology (HP:0003043) help
..expandAbnormal sternum morphology (HP:0000766) help
..expandAbnormal thoracic spine morphology (HP:0100711) help
..expandAplasia/Hypoplasia involving bones of the thorax (HP:0006711) help
..expandChest pain (HP:0100749) help
..expandIntercostal muscle weakness (HP:0004878) help
..expandShort thorax (HP:0010306) help
..expandThoracic hypoplasia (HP:0005257) 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:0100656HP:0100656Thoracoabdominal wall defect0 CL E G H
HP:0100656HP:0100657Thoracoabdominal eventration1 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.