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Goldenhar Syndrome MeSH Descriptor Data 2025


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
Goldenhar Syndrome Preferred
Goldenhar Syndrome with Ipsilateral Radial Defect Related
Hemifacial Microsomia Narrower
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