MeSH Browser

MeSH Heading: Orofaciodigital Syndromes
Tree 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
Unique ID: D009958
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D009958
Annotation: do not use /‌congen & do not coord with INFANT, NEWBORN, DISEASES
Scope Note: 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.
Entry Term(s): Dysplasia Linguofacialis; Gorlin-Psaume Syndrome; Mohr Syndrome; Oral-Facial-Digital Syndrome; Oral-Facial-Digital Syndrome, Type 1; Oral-Facial-Digital Syndrome, Type 2; Oral-Facial-Digital Syndrome, Type I; Oral-Facial-Digital Syndrome, Type II; Oro-Facio-Digital Syndrome; Orodigitofacial Dysostosis; Orodigitofacial Syndrome; Orofaciodigital Syndrome; Orofaciodigital Syndrome 2; Orofaciodigital Syndrome I; Orofaciodigital Syndrome II; Orofaciodigital Syndrome Type1; Papillon-Leage and Psaume Syndrome; Papillon-League-Psaume Syndrome
Public MeSH Note: 2027; for OROFACIODIGITAL SYNDROME TYPE1 see OROFACIODIGITAL SYNDROME TYPE1(NM) 2010-2026 for ORAL-FACIAL-DIGITAL SYNDROME, TYPE 2 see ORAL-FACIAL-DIGITAL SYNDROME, TYPE 2 (NM) 2010-2026; was OROFACIODIGITAL SYNDROME see under ABNORMALITIES, MULTIPLE 1975-78
Online Note: use OROFACIODIGITAL SYNDROMES to search OROFACIODIGITAL SYNDROME 1966-78(as Prov 1966-74)
History Note: 2027 (1979); for OROFACIODIGITAL SYNDROME TYPE1 use OROFACIODIGITAL SYNDROME TYPE1(NM) 2010-2016; for ORAL-FACIAL-DIGITAL SYNDROME, TYPE 2 use ORAL-FACIAL-DIGITAL SYNDROME, TYPE 2 (NM) 2010-2026; was OROFACIODIGITAL SYNDROME see under ABNORMALITIES, MULTIPLE 1975-78; was OROFACIODIGITAL SYNDROME 1964-74 (Prov)
Date Introduced: 1991/01/01
Last Updated: 2027/01/01

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)

Musculoskeletal Diseases [C05]
- Bone Diseases [C05.116]
  - Bone Diseases, Developmental [C05.116.099]
    - Dysostoses [C05.116.099.370]

Musculoskeletal Diseases [C05]
- Musculoskeletal Abnormalities [C05.660]
  - Craniofacial Abnormalities [C05.660.207]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
  - Abnormalities, Multiple [C16.131.077]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
  - Chromosome Disorders [C16.131.260]
    - Sex Chromosome Disorders [C16.131.260.830]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Congenital Abnormalities [C16.131]
  - Musculoskeletal Abnormalities [C16.131.621]
    - Craniofacial Abnormalities [C16.131.621.207]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Chromosome Disorders [C16.320.180]
    - Sex Chromosome Disorders [C16.320.180.830]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]

Orofaciodigital Syndromes Preferred

Concept UI: M0015438
Scope Note: 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.
Terms: Orofaciodigital Syndromes Preferred Term
Term UI T029455
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1964); Dysplasia Linguofacialis
Term UI T842207
Date04/18/2013
LexicalTag NON
ThesaurusID NLM (2014); Oral-Facial-Digital Syndrome
Term UI T842206
Date04/18/2013
LexicalTag NON
ThesaurusID NLM (2014); Oro-Facio-Digital Syndrome
Term UI T842208
Date04/18/2013
LexicalTag NON
ThesaurusID NLM (2014); Orodigitofacial Dysostosis
Term UI T842209
Date04/18/2013
LexicalTag NON
ThesaurusID NLM (2014); Orodigitofacial Syndrome
Term UI T842210
Date04/18/2013
LexicalTag NON
ThesaurusID NLM (2014); Orofaciodigital Syndrome
Term UI T842211
Date04/18/2013
LexicalTag NON
ThesaurusID NLM (2014)

Mohr Syndrome Narrower

Papillon-Leage and Psaume Syndrome Narrower

Orofaciodigital Syndromes MeSH Descriptor Data 2027