Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormal pulmonary interstitial morphology (HP:0006530)

Parent Node:
Pulmonary interstitial high-resolution computed tomography abnormality (HP:0025389)

..Starting node
..Reticular pattern on pulmonary HRCT (HP:0025390)

Term ID:

25390

Name:

Reticular pattern on pulmonary HRCT

Synonym:

Definition:

On pulmonary high-resolution computed tomography, reticular pattern is characterised by innumerable interlacing shadows suggesting a mesh.

Comments:

Reference:

HP:0025390

Genes and Diseases:

Child Nodes:

Sister Nodes:

Combined cystic and ground-glass pattern on pulmonary HRCT (HP:0025395)

Crazy paving pattern (HP:0025391)

Cystic pattern on pulmonary HRCT (HP:0025394)

Decreased attenuation pattern on pulmonary HRCT (HP:0025396)

Ground-glass opacification (HP:0025179)

Interlobular septal thickening (HP:0030879)

Mosaic attenuation pattern on pulmonary HRCT (HP:0025397)

Nodular pattern on pulmonary HRCT (HP:0025392)

Reticulonodular pattern on pulmonary HRCT (HP:0025393)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	ABCA3 CL E G H	21	33	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent	147
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	ABCA3 CL E G H	21	33	OMIM:610921	Surfactant metabolism dysfunction, pulmonary, 3		147
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	ATP11A CL E G H	23250	13552	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	DPP9 CL E G H	91039	18648	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	DSP CL E G H	1832	3052	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent	747
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	FAM13A CL E G H	10144	19367	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	MUC5B CL E G H	727897	7516	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent	133
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	PARN CL E G H	5073	8609	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent	26
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	RTEL1 CL E G H	51750	15888	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent	77
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	SFTPA1 CL E G H	653509	10798	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent	19
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	SFTPA2 CL E G H	729238	10799	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent	10
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	SFTPC CL E G H	6440	10802	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent	33
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	STN1 CL E G H	79991	26200	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent	2
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	TERC CL E G H	7012	11727	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent	48
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	TERT CL E G H	7015	11730	ORPHA:2032	Idiopathic pulmonary fibrosis	HP:0040282 - Frequent	238
HP:0025390	HP:0025390	Reticular pattern on pulmonary HRCT	0	TERT CL E G H	7015	11730	OMIM:614742	PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1		238

Genes (14) :ABCA3 ATP11A DPP9 DSP FAM13A MUC5B PARN RTEL1 SFTPA1 SFTPA2 SFTPC STN1 TERC TERT

Diseases (3) :ORPHA:2032 OMIM:610921 OMIM:614742

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

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