Human Phenotype Ontology 
Grandparent Node:
expandAbnormal skull morphology (HP:0000929)help
Parent Node:
expandAbnormality of the skull base (HP:0002693)help
..Starting node
..expandElevated imprint of the transverse sinuses (HP:0000930)help
Term ID: 930
Name: Elevated imprint of the transverse sinuses
Synonym: Elevated imprint of occipital bone over the transverse sinuses; Elevated imprint of posterior skull bones over the transverse sinuses; Thinning and bulging of occipital bone over the transverse sinuses; Thinning and bulging of posterior skull bones over the transverse sinuses
Definition:
Comments:
Reference: HP:0000930
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal posterior cranial fossa morphology (HP:0000932) help
..expandCleft in skull base (HP:0009752) help
..expandSclerosis of skull base (HP:0002694) help
..expandThick skull base (HP:0002737) 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:0000930HP:0000930Elevated imprint of the transverse sinuses0 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.