MeSH Browser

MeSH Heading: Weill-Marchesani Syndrome
Tree Number(s): C05.116.099.343.957; C11.270.921; C16.131.077.941; C16.320.290.842; C17.300.899
Unique ID: D056846
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D056846
Scope Note: Rare congenital disorder of connective tissue characterized by brachydactyly, joint stiffness, childhood onset of ocular abnormalities (e.g., microspherophakia, ECTOPIA LENTIS; GLAUCOMA), and proportionate short stature. Cardiovascular anomalies are occasionally seen.
Entry Term(s): Congenital Mesodermal Dysmorphodystrophy; GEMSS; Glaucoma-Lens Ectopia-Microspherophakia-Stiffness-Shortness Syndrome; Marchesani Syndrome; Marchesani-Weill Syndrome; Mesodermal Dysmorphodystrophy, Congenital; Spherophakia Brachymorphia Syndrome; Spherophakia-Brachymorphia Syndrome; Weill Marchesani Syndrome; Weill-Marchesani Syndrome, Autosomal Dominant; Weill-Marchesani Syndrome, Autosomal Recessive
See Also: Marfan Syndrome
Public MeSH Note: 2010
History Note: 2010
Date Established: 2010/01/01
Date of Entry: 2009/07/06
Revision Date: 2015/06/23

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Concept UI: M0529438
Scope Note: Rare congenital disorder of connective tissue characterized by brachydactyly, joint stiffness, childhood onset of ocular abnormalities (e.g., microspherophakia, ECTOPIA LENTIS; GLAUCOMA), and proportionate short stature. Cardiovascular anomalies are occasionally seen.
Terms: Weill-Marchesani Syndrome Preferred Term
Term UI T734979
Date02/12/2009
LexicalTag EPO
ThesaurusID; Marchesani Syndrome
Term UI T842680
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Weill Marchesani Syndrome
Term UI T734980
Date02/12/2009
LexicalTag EPO
ThesaurusID NLM (2010); Mesodermal Dysmorphodystrophy, Congenital
Term UI T734982
Date02/12/2009
LexicalTag NON
ThesaurusID; Spherophakia Brachymorphia Syndrome
Term UI T734981
Date02/12/2009
LexicalTag NON
ThesaurusID; Spherophakia-Brachymorphia Syndrome
Term UI T842681
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Congenital Mesodermal Dysmorphodystrophy
Term UI T842679
Date04/18/2013
LexicalTag NON
ThesaurusID GHR (2014); Marchesani-Weill Syndrome
Term UI T748782
Date04/06/2009
LexicalTag NON
ThesaurusID NLM (2010)

Weill-Marchesani Syndrome MeSH Descriptor Data 2023