MeSH Browser

MeSH Heading: Goldenhar Syndrome
Tree Number(s): C05.116.099.370.231.576.410; C05.660.207.231.576.410; C16.131.621.207.231.576.410
Unique ID: D006053
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D006053
Scope Note: Mandibulofacial dysostosis with congenital eyelid dermoids.
Entry Term(s): Craniofacial Microsomia; Facioauriculovertebral Dysplasia; Facioauriculovertebral Sequence; First and Second Branchial Arch Syndrome; First and Second Pharyngeal Arch Syndromes; Goldenhar Disease; Goldenhar Syndrome with Ipsilateral Radial Defect; Goldenhar-Gorlin Syndrome; Hemifacial Microsomia; Hemifacial Microsomia with Radial Defects; Lateral Facial Dysplasia; Microsomia Hemifacial Radial Defects; Moeschler Clarren Syndrome; OAVS with Radial Defect; Oculoauriculovertebral Dysplasia; Oculoauriculovertebral Spectrum; Oculoauriculovertebral Spectrum with Radial Defect; Oculoauriculovertebral Syndrome; Oral-Mandibular-Auricular Syndrome; Otomandibular Dysostosis
Previous Indexing: Abnormalities, Multiple (1968-1978); Mandibulofacial Dysostosis (1966-1978)
Public MeSH Note: 91; was see under MANDIBULOFACIAL DYSOSTOSIS 1979-90
History Note: 91(79); was see under MANDIBULOFACIAL DYSOSTOSIS 1979-90
Date Established: 1991/01/01
Date of Entry: 1978/05/19
Revision Date: 2017/06/20

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)

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ethnology (EH)

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microbiology (MI)

mortality (MO)

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pathology (PA)

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prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Goldenhar Syndrome MeSH Descriptor Data 2025