Weill-Marchesani Syndrome

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Weill-Marchesani Syndrome

"Weill-Marchesani Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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.

Descriptor ID	D056846
MeSH Number(s)	C05.116.099.343.957 C05.116.099.875 C11.270.921 C16.131.077.941 C16.320.290.842 C16.320.887 C17.300.899
Concept/Terms	Weill-Marchesani Syndrome Weill-Marchesani Syndrome Syndrome, Weill-Marchesani Mesodermal Dysmorphodystrophy, Congenital Congenital Mesodermal Dysmorphodystrophies Congenital Mesodermal Dysmorphodystrophy Dysmorphodystrophies, Congenital Mesodermal Dysmorphodystrophy, Congenital Mesodermal Mesodermal Dysmorphodystrophies, Congenital Weill Marchesani Syndrome Marchesani-Weill Syndrome Marchesani Weill Syndrome Marchesani-Weill Syndromes Syndrome, Marchesani-Weill Syndromes, Marchesani-Weill Spherophakia Brachymorphia Syndrome Spherophakia Brachymorphia Syndromes Syndrome, Spherophakia Brachymorphia Syndromes, Spherophakia Brachymorphia Weill-Marchesani Syndrome, Autosomal Recessive Weill-Marchesani Syndrome, Autosomal Recessive Weill Marchesani Syndrome, Autosomal Recessive Weill-Marchesani Syndrome, Autosomal Dominant Weill-Marchesani Syndrome, Autosomal Dominant Weill Marchesani Syndrome, Autosomal Dominant

Below are MeSH descriptors whose meaning is more general than "Weill-Marchesani Syndrome".

Diseases [C]
Musculoskeletal Diseases [C05]
Bone Diseases [C05.116]
Bone Diseases, Developmental [C05.116.099]
Dwarfism [C05.116.099.343]
Weill-Marchesani Syndrome [C05.116.099.343.957]
Weill-Marchesani Syndrome [C05.116.099.875]
Eye Diseases [C11]
Eye Diseases, Hereditary [C11.270]
Weill-Marchesani Syndrome [C11.270.921]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
Weill-Marchesani Syndrome [C16.131.077.941]
Genetic Diseases, Inborn [C16.320]
Eye Diseases, Hereditary [C16.320.290]
Weill-Marchesani Syndrome [C16.320.290.842]
Weill-Marchesani Syndrome [C16.320.887]
Skin and Connective Tissue Diseases [C17]
Connective Tissue Diseases [C17.300]
Weill-Marchesani Syndrome [C17.300.899]

Below are MeSH descriptors whose meaning is related to "Weill-Marchesani Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Weill-Marchesani Syndrome".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Weill-Marchesani Syndrome" by people in UAMS Profiles by year, and whether "Weill-Marchesani Syndrome" was a major or minor topic of these publications.

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