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Descriptor English: Orofaciodigital Syndromes
Descriptor Spanish: Síndromes Orofaciodigitales
Descriptor Portuguese: Síndromes Orofaciodigitais
Descriptor French: Syndromes oro-facio-digitaux
Entry term(s): Dysplasia Linguofacialis
Gorlin Psaume Syndrome
Gorlin-Psaume Syndrome
Mohr Syndrome
Oral Facial Digital Syndrome, Type I
Oral Facial Digital Syndrome, Type II
Oral-Facial-Digital Syndrome
Oral-Facial-Digital Syndrome, Type I
Oral-Facial-Digital Syndrome, Type II
Oro-Facio-Digital Syndrome
Orodigitofacial Dysostosis
Orodigitofacial Syndrome
Orofaciodigital Syndrome
Orofaciodigital Syndrome I
Orofaciodigital Syndrome II
Orofaciodigital Syndrome IIs
Orofaciodigital Syndrome Is
Papillon Leage and Psaume Syndrome
Papillon-Leage and Psaume Syndrome
Syndrome, Gorlin-Psaume
Syndrome, Mohr
Syndrome, Orofaciodigital
Syndromes, Orofaciodigital
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
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D009958
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.
Annotation: do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 79; 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: 79; was OROFACIODIGITAL SYNDROME see under ABNORMALITIES, MULTIPLE 1975-78; was OROFACIODIGITAL SYNDROME 1964-74 (Prov)
DeCS ID: 10135
Unique ID: D009958
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1991/01/01
Date of Entry: 1999/01/01
Revision Date: 2016/06/30
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.
Preferred term Orofaciodigital Syndromes
Entry term(s) Dysplasia Linguofacialis
Oral-Facial-Digital Syndrome
Oro-Facio-Digital Syndrome
Orodigitofacial Dysostosis
Orodigitofacial Syndrome
Orofaciodigital Syndrome
Syndrome, Orofaciodigital
Syndromes, Orofaciodigital
Papillon-Leage and Psaume Syndrome - Narrower
Concept UI M0015440
Preferred term Papillon-Leage and Psaume Syndrome
Entry term(s) Gorlin Psaume Syndrome
Gorlin-Psaume Syndrome
Oral Facial Digital Syndrome, Type I
Oral-Facial-Digital Syndrome, Type I
Orofaciodigital Syndrome I
Orofaciodigital Syndrome Is
Papillon Leage and Psaume Syndrome
Syndrome, Gorlin-Psaume
Mohr Syndrome - Narrower
Concept UI M0015437
Preferred term Mohr Syndrome
Entry term(s) Oral Facial Digital Syndrome, Type II
Oral-Facial-Digital Syndrome, Type II
Orofaciodigital Syndrome II
Orofaciodigital Syndrome IIs
Syndrome, Mohr



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