syndrome that is characterized by incomplete development of the ear, nose, soft palate, lip, and mandible. It is associated with anomalous development of the first branchial arch and second branchial arch
Goldenhar syndrome is a head and neck disease[1]. It draws 188 Wikipedia views per month (head_and_neck_disease category, ranking #12 of 92).[2]
Key Facts
Goldenhar syndrome's instance of is recorded as head and neck disease[3].
Goldenhar syndrome's instance of is recorded as developmental defect during embryogenesis[4].
Goldenhar syndrome's instance of is recorded as class of disease[5].
Maurice Goldenhar is named after Goldenhar syndrome[6].
Goldenhar syndrome's subclass of is recorded as syndrome[7].
Goldenhar syndrome's subclass of is recorded as Hemifacial microsomia[8].
Goldenhar syndrome's subclass of is recorded as skull cancer[9].
Goldenhar syndrome's subclass of is recorded as cornea cancer[10].
Goldenhar syndrome's subclass of is recorded as bulbar conjunctival dermoid or conjunctival dermolipoma[11].
Goldenhar syndrome's subclass of is recorded as syndromic corneal dystrophy[12].
Goldenhar syndrome's subclass of is recorded as lens shape anomaly[13].
Goldenhar syndrome's subclass of is recorded as syndromic palpebral coloboma[14].
Goldenhar syndrome's subclass of is recorded as syndromic developmental defect of the eye[15].
Goldenhar syndrome's subclass of is recorded as Pierre robin syndrome associated with branchial archs anomalies[16].
Goldenhar syndrome's subclass of is recorded as oculo-auriculo-vertebral spectrum[17].
Goldenhar syndrome's Commons category is recorded as Goldenhar syndrome[18].
Goldenhar syndrome's MeSH descriptor ID is recorded as D006053[19].
Goldenhar syndrome's OMIM ID is recorded as 164210[20].
Goldenhar syndrome's DiseasesDB is recorded as 31292[21].
Goldenhar syndrome's Freebase ID is recorded as /m/097lh2[22].
Goldenhar syndrome's MeSH tree code is recorded as C05.116.099.370.231.576.410[23].
Goldenhar syndrome's MeSH tree code is recorded as C05.660.207.231.576.410[24].
Goldenhar syndrome's MeSH tree code is recorded as C16.131.621.207.231.576.410[25].
Goldenhar syndrome's Disease Ontology ID is recorded as DOID:2907[26].
Goldenhar syndrome's Encyclopædia Britannica Online ID is recorded as topic/Goldenhar-syndrome[27].
Why It Matters
Goldenhar syndrome draws 188 Wikipedia views per month (head_and_neck_disease category, ranking #12 of 92).[2] It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[28] It is known by 26 alternative names across languages and contexts.[29]
References
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Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.
APA4ort.xyz Knowledge Graph. (2026). Goldenhar syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/goldenhar-syndrome