Human Phenotype Ontology 
Grandparent Node:
expandPulmonary interstitial high-resolution computed tomography abnormality (HP:0025389)help
Grandparent Node:
expandPulmonary opacity (HP:0031457)help
Parent Node:
expandGround-glass opacification (HP:0025179)help
..Starting node
..expandCentrilobular ground-glass opacification on pulmonary HRCT (HP:0025180)help
Term ID: 25180
Name: Centrilobular ground-glass opacification on pulmonary HRCT
Synonym: Centrilobular groundglass opacification; Centrilobular groundglass opacity
Definition: A hazy area of increased attenuation in centrilobular areas of the lung with preserved bronchial and vascular markings seen on a computer tomography scan. Centrilobular refers to a location that is central within secondary pulmonary lobules.
Comments:
Reference: HP:0025180
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025180HP:0025180Centrilobular ground-glass opacification on pulmonary HRCT0BMPR2 CL E G H6591078OMIM:265450PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT; PVOD1525
HP:0025180HP:0025180Centrilobular ground-glass opacification on pulmonary HRCT0EIF2AK4 CL E G H44027519687ORPHA:199241Pulmonary capillary hemangiomatosisHP:0040282 - Frequent40
HP:0025180HP:0025180Centrilobular ground-glass opacification on pulmonary HRCT0EIF2AK4 CL E G H44027519687OMIM:234810PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE; PVOD240


Genes (2) :BMPR2 EIF2AK4

Diseases (3) :OMIM:265450 ORPHA:199241 OMIM:234810
 

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