Human Phenotype Ontology 
Grandparent Node:
expandAbnormal pulmonary interstitial morphology (HP:0006530)help
Parent Node:
expandPulmonary interstitial high-resolution computed tomography abnormality (HP:0025389)help
..Starting node
..expandCystic pattern on pulmonary HRCT (HP:0025394)help
Term ID: 25394
Name: Cystic pattern on pulmonary HRCT
Synonym:
Definition: On pulmonary high-resolution computed tomography, the cystic pattern is composed by well-defined, round and circumscribed air-containing parenchymal spaces with a well-defined wall and interface with normal lung. The wall of the cysts may be uniform or varied in thickness, but usually is thin (less than 2 mm) and occurs without associated emphysema.
Comments:
Reference: HP:0025394
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCombined cystic and ground-glass pattern on pulmonary HRCT (HP:0025395) help
..expandCrazy paving pattern (HP:0025391) help
..expandDecreased attenuation pattern on pulmonary HRCT (HP:0025396) help
..expandGround-glass opacification (HP:0025179) help
..expandInterlobular septal thickening (HP:0030879) help
..expandMosaic attenuation pattern on pulmonary HRCT (HP:0025397) help
..expandNodular pattern on pulmonary HRCT (HP:0025392) help
..expandReticular pattern on pulmonary HRCT (HP:0025390) help
..expandReticulonodular pattern on pulmonary HRCT (HP:0025393) 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:0025394HP:0025394Cystic pattern on pulmonary HRCT0ABCA3 CL E G H2133OMIM:610921Surfactant metabolism dysfunction, pulmonary, 3147
HP:0025394HP:0025394Cystic pattern on pulmonary HRCT0NKX2-1 CL E G H708011825OMIM:610978Choreoathetosis, hypothyroidism, and neonatal respiratory distress51
HP:0025394HP:0025394Cystic pattern on pulmonary HRCT0SFTPC CL E G H644010802OMIM:610913Surfactant metabolism dysfunction, pulmonary, 233


Genes (3) :ABCA3 NKX2-1 SFTPC

Diseases (3) :OMIM:610921 OMIM:610978 OMIM:610913
 

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