Orofaciodigital Syndromes

"Orofaciodigital Syndromes" 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

Two syndromes of oral, facial, and digital malformations. Type I (Papillon-Leage and Psaume syndrome, Gorlin-Psaume syndrome) is inherited as an X-linked dominant trait and is found only in females and XXY males. Type II (Mohr syndrome) is inherited as an autosomal recessive trait.

Descriptor ID	D009958
MeSH Number(s)	C05.116.099.370.652 C05.660.207.700 C16.131.077.676 C16.131.260.830.670 C16.131.621.207.700 C16.320.180.830.670 C16.320.714
Concept/Terms	Orofaciodigital Syndromes Orofaciodigital Syndromes Syndrome, Orofaciodigital Syndromes, Orofaciodigital Dysplasia Linguofacialis Orofaciodigital Syndrome Orodigitofacial Dysostosis Orodigitofacial Syndrome Oral-Facial-Digital Syndrome Oro-Facio-Digital Syndrome Papillon-Leage and Psaume Syndrome Papillon-Leage and Psaume Syndrome Papillon Leage and Psaume Syndrome Oral-Facial-Digital Syndrome, Type I Oral Facial Digital Syndrome, Type I Orofaciodigital Syndrome I Orofaciodigital Syndrome Is Gorlin-Psaume Syndrome Gorlin Psaume Syndrome Syndrome, Gorlin-Psaume Mohr Syndrome Mohr Syndrome Syndrome, Mohr Orofaciodigital Syndrome II Orofaciodigital Syndrome IIs Oral-Facial-Digital Syndrome, Type II Oral Facial Digital Syndrome, Type II

Below are MeSH descriptors whose meaning is more general than "Orofaciodigital Syndromes".

Diseases [C]
Musculoskeletal Diseases [C05]
Bone Diseases [C05.116]
Bone Diseases, Developmental [C05.116.099]
Dysostoses [C05.116.099.370]
Orofaciodigital Syndromes [C05.116.099.370.652]
Musculoskeletal Abnormalities [C05.660]
Craniofacial Abnormalities [C05.660.207]
Orofaciodigital Syndromes [C05.660.207.700]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
Orofaciodigital Syndromes [C16.131.077.676]
Chromosome Disorders [C16.131.260]
Sex Chromosome Disorders [C16.131.260.830]
Orofaciodigital Syndromes [C16.131.260.830.670]
Musculoskeletal Abnormalities [C16.131.621]
Craniofacial Abnormalities [C16.131.621.207]
Orofaciodigital Syndromes [C16.131.621.207.700]
Genetic Diseases, Inborn [C16.320]
Chromosome Disorders [C16.320.180]
Sex Chromosome Disorders [C16.320.180.830]
Orofaciodigital Syndromes [C16.320.180.830.670]
Orofaciodigital Syndromes [C16.320.714]

Below are MeSH descriptors whose meaning is related to "Orofaciodigital Syndromes".

Below are MeSH descriptors whose meaning is more specific than "Orofaciodigital Syndromes".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Orofaciodigital Syndromes" by people in this website by year, and whether "Orofaciodigital Syndromes" was a major or minor topic of these publications.

Bar chart showing 2 publications over 2 distinct years, with a maximum of 1 publications in 2016 and 2017

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2016	1	0	1
2017	1	0	1

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Pazour, Gregory

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