Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the fontanelles or cranial sutures (HP:0000235)help
Parent Node:
expandAbnormality of cranial sutures (HP:0011329)help
..Starting node
..expandWidely patent coronal suture (HP:0005442)help
Term ID: 5442
Name: Widely patent coronal suture
Synonym:
Definition: The presence of a coronal suture (the cranial suture that separates the frontal and parietal bones) that is not ossified but rather wide open at an age when it is normally closed.
Comments:
Reference: HP:0005442
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of the metopic suture (HP:0005556) help
..expandAccessory cranial suture (HP:0012800) help
..expandCraniosynostosis (HP:0001363) help
..expandDelayed cranial suture closure (HP:0000270) help
..expandRidged cranial sutures (HP:0010823) help
..expandSclerotic cranial sutures (HP:0005441) help
..expandWide cranial sutures (HP:0010537) help
..expandWidely patent sagittal suture (HP:0005476) help
..expandWormian bones (HP:0002645) 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:0005442HP:0005442Widely patent coronal suture0COL11A1 CL E G H13012186OMIM:228520Fibrochondrogenesis 1.215


Genes (1) :COL11A1

Diseases (1) :OMIM:228520
 

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