Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of cranial sutures (HP:0011329)help
Grandparent Node:
expandAbnormality of the forehead (HP:0000290)help
Parent Node:
expandAbnormality of the metopic suture (HP:0005556)help
..Starting node
..expandMetopic suture patent to nasal root (HP:0005495)help
Term ID: 5495
Name: Metopic suture patent to nasal root
Synonym:
Definition: The frontal suture divides the two halves of the frontal bone in infants and usually fuses by the age of six years. The suture runs from the bregma (the point on the skull at which the coronal suture is intersected perpendicularly by the sagittal suture) to the nasion or nasal root. This term applies if the suture is widely patent from bregma to nasal root.
Comments:
Reference: HP:0005495
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMetopic depression (HP:0011223) help
..expandMetopic synostosis (HP:0011330) help
..expandProminent metopic ridge (HP:0005487) 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:0005495HP:0005495Metopic suture patent to nasal root0SETBP1 CL E G H2604015573OMIM:269150Schinzel-Giedion midface-retraction syndrome.143


Genes (1) :SETBP1

Diseases (1) :OMIM:269150
 

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