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 type of cornea cancer[10].
Goldenhar syndrome is a type of bulbar conjunctival dermoid or conjunctival dermolipoma[11].
Goldenhar syndrome is a type of syndromic corneal dystrophy[12].
Goldenhar syndrome is a type of lens shape anomaly[13].
Goldenhar syndrome is a type of syndromic palpebral coloboma[14].
Goldenhar syndrome is a type of syndromic developmental defect of the eye[15].
Goldenhar syndrome is a type of Pierre robin syndrome associated with branchial archs anomalies[16].
Goldenhar syndrome is a type of oculo-auriculo-vertebral spectrum[17].
Goldenhar syndrome's Commons category is recorded as Goldenhar syndrome[18].
Goldenhar syndrome's ICD-9-CM is recorded as 759.89[19].
Goldenhar syndrome's NCI Thesaurus ID is recorded as C84740[20].
Goldenhar syndrome's health specialty is recorded as medical genetics[21].
Goldenhar syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2907[22].
Goldenhar syndrome's exact match is recorded as http://identifiers.org/doid/DOID:2907[23].
Goldenhar syndrome's exact match is recorded as http://purl.obolibrary.org/obo/HP_0011332[24].
Goldenhar syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_374[25].
Goldenhar syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[26].
Why It Matters
Goldenhar syndrome draws 190 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.[27] It is known by 26 alternative names across languages and contexts.[28]
References
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APA4ort.xyz Knowledge Graph. (2026). Goldenhar syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/goldenhar-syndrome
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