Craniofacial microsomia

rare

Identifiers: MONDO:0015397 Orphanet:141132 Orphanet:141136 Orphanet:374
Part of: Neurocristopathy Oculoauriculovertebral spectrum with radial defects Syndromic disease
Also known as: Expanded spectrum hemifacial microsomia · Expanded spectrum of hemifacial microsomia · facioauriculovertebral dysplasia · first branchial arch syndrome · Goldenhar disease

Subtypes

Disease	ID	Subtypes	Genes
Craniofacial microsomia 1	MONDO:0958175		SF3B2
Craniofacial microsomia 2	MONDO:0958194		FOXI3

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