MeSH Browser

MeSH Heading: Mobius Syndrome
Tree Number(s): C07.465.299.825; C10.292.319.825; C10.292.562.700.375.750; C11.590.436.400.750; C16.131.077.578; C16.614.595
Unique ID: D020331
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D020331
Scope Note: A syndrome of congenital facial paralysis, frequently associated with abducens palsy and other congenital abnormalities including lingual palsy, clubfeet, brachial disorders, cognitive deficits, and pectoral muscle defects. Pathologic findings are variable and include brain stem nuclear aplasia, facial nerve aplasia, and facial muscle aplasia, consistent with a multifactorial etiology. (Adams et al., Principles of Neurology, 6th ed, p1020)
Entry Term(s): Congenital Oculofacial Paralysis, Moebius; Congenital Ophthalmoplegia and Facial Paresis; Moebius Congenital Oculofacial Paralysis; Moebius Sequence; Moebius Spectrum; Moebius Syndrome; Möbius Sequence
Previous Indexing: Facial Paralysis (1966-1999)
See Also: Facial Paralysis
Public MeSH Note: 2000: see FACIAL PARALYSIS 1997-1999
History Note: 2000; use FACIAL PARALYSIS 1997-1999
Date Established: 2000/01/01
Date of Entry: 1999/11/08
Revision Date: 2022/04/19

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: M0008126
Scope Note: A syndrome of congenital facial paralysis, frequently associated with abducens palsy and other congenital abnormalities including lingual palsy, clubfeet, brachial disorders, cognitive deficits, and pectoral muscle defects. Pathologic findings are variable and include brain stem nuclear aplasia, facial nerve aplasia, and facial muscle aplasia, consistent with a multifactorial etiology. (Adams et al., Principles of Neurology, 6th ed, p1020)
Terms: Mobius Syndrome Preferred Term
Term UI T015753
Date09/13/1995
LexicalTag NON
ThesaurusID; Congenital Oculofacial Paralysis, Moebius
Term UI T370492
Date10/12/1999
LexicalTag NON
ThesaurusID NLM (2000); Möbius Sequence
Term UI T842034
Date04/18/2013
LexicalTag NON
ThesaurusID; Congenital Ophthalmoplegia and Facial Paresis
Term UI T751794
Date05/28/2009
LexicalTag NON
ThesaurusID; Moebius Sequence
Term UI T812123
Date11/15/2011
LexicalTag NON
ThesaurusID; Moebius Spectrum
Term UI T842033
Date04/18/2013
LexicalTag NON
ThesaurusID; Moebius Syndrome
Term UI T015752
Date09/13/1995
LexicalTag NON
ThesaurusID; Moebius Congenital Oculofacial Paralysis
Term UI T370493
Date10/12/1999
LexicalTag NON
ThesaurusID

Mobius Syndrome MeSH Descriptor Data 2024