cystic

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Related to cystic: cystic fibrosis, cystic acne, cystic hyperplasia, Cysts

cys·tic

(sĭs′tĭk)

adj.

1. Of, relating to, or having characteristics of a cyst.

2. Having or containing cysts or a cyst.

3. Enclosed in a cyst.

4. Anatomy Of, relating to, or involving the gallbladder or urinary bladder.

American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.

cystic

(ˈsɪstɪk)

adj

1. (Biology) of, relating to, or resembling a cyst

2. (Biology) having or enclosed within a cyst; encysted

3. (Anatomy) relating to the gall bladder or urinary bladder

Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014

cys•tic

(ˈsɪs tɪk)

adj.

1. pertaining to, of the nature of, or having a cyst or cysts; encysted.

2. belonging or pertaining to the urinary bladder or gallbladder.

[1625–35]

ThesaurusAntonymsRelated WordsSynonymsLegend:

Switch to new thesaurus

Adj.	1.	cystic - of or relating to a normal cyst (as the gallbladder or urinary bladder)
	2.	cystic - of or relating to or resembling a cyst

Translations

κυστικός

cystic

[ˈsɪstɪk]

A. ADJ → cístico

B. CPD cystic fibrosis N → fibrosis f cística

Collins Spanish Dictionary - Complete and Unabridged 8th Edition 2005 © William Collins Sons & Co. Ltd. 1971, 1988 © HarperCollins Publishers 1992, 1993, 1996, 1997, 2000, 2003, 2005

cys·tic

a. cístico-a, rel. a la vesícula biliar o la vejiga urinaria;

___ duct → conducto ___.

English-Spanish Medical Dictionary © Farlex 2012

cystic

adj quístico; (related to bladder or gallbladder) cístico

References in periodicals archive ?

Bethesda, MD, August 21, 2019 --(PR.com)-- The Cystic Fibrosis Foundation Challenges the Metro DC Corporate Community to Join in their Pursuit to End Cystic Fibrosis (CF) through the 9th Annual Metro DC CF Cycle for Life Corporate Challenge.

CF Cycle for Life Corporate Challenge 2019

ENPNewswire-August 12, 2019--KU Leuven: Researchers use CRISPR/Cas to repair two mutations of the cystic fibrosis gene

KU Leuven: Researchers use CRISPR/Cas to repair two mutations of the cystic fibrosis gene

Global Banking News-June 27, 2019-Aridis Pharmaceuticals awarded FDA's ODD for AR-501 for cystic fibrosis

Aridis Pharmaceuticals awarded FDA's ODD for AR-501 for cystic fibrosis

M2 EQUITYBITES-June 27, 2019-Aridis Pharmaceuticals awarded FDA's ODD for AR-501 for cystic fibrosis

Aridis Pharmaceuticals awarded FDA's ODD for AR-501 for cystic fibrosis

M2 PHARMA-June 27, 2019-Aridis Pharmaceuticals awarded FDA's ODD for AR-501 for cystic fibrosis

Aridis Pharmaceuticals awarded FDA's ODD for AR-501 for cystic fibrosis

Cystic nephroma is a mixed mesenchymal and epithelial neoplasm of the kidney which has a benign nature and tends to grow slowly (1).

The Largest Cystic Nephroma Treated by Laparoscopic Nephron-sparing Surgery: A Case Report and Review of the Literature/Laparoskopik Nefron Koruyucu Cerrahi ile Tedavi Edilen En Buyuk Kistik Nefroma Olgusu: Olgu Sunumu Esliginde Literaturun Gozden Gecirilmesi

Elle Morris, from Nantwich, who died aged 11 while awaiting cystic fibrosis drug Orkambi, is the face of a poster campaign pleading for others to get the life-saving treatment which she was denied.

Elle, who died aged 11, is face of campaign

Summary: Acquired cystic kidney disease occurs both, in adults and children.

Acquired Cystic Kidney Disease Treatment Market Offered in New Research Forecasted through 2028

Cystic fibrosis is a genetic condition that causes breathing difficulties and coughing up mucus from frequent lung infections.

Reading Hospital opening Cystic Fibrosis clinic

Cystic fibrosis is an autosomal recessive disorder.

Skin Findings in Cystic Fibrosis Cases

Eloxx Pharmaceuticals announced "positive" data demonstrating that ELX-02 showed significant increases in CFTR functional assay and mRNA levels across multiple CFTR nonsense mutations in cystic fibrosis patient-derived organoids.