General Information of Disease (ID: DIS0SIK5)

Disease Name Oculoauriculovertebral spectrum with radial defects
Synonyms
Goldenhar syndrome with ipsilateral radial defect; oculoauriculovertebral spectrum with radial defect; Moeschler Clarren syndrome; hemifacial microsomia with radial defects; microsomia hemifacial radial defects; Oavs with radial defect; hemifacial microsomia-radial defects syndrome; Moeschler-Clarren syndrome
Definition
Oculoauriculovertebral spectrum (OAVS) with radial defects is a rare branchial arches and limb primordia development disorder characterized by variable degrees of uni- or bilateral craniofacial malformation and radial defects that result in extremely variable phenotypic manifestations. Characteristic features include low postnatal weight, short stature, vertebral defects, hearing loss, and facial dysmorphism (incl. facial asymmetry, external, middle, and inner ear malformations, orofacial clefts, and mandibular hypoplasia). These features are invariably associated with radial defects, such as preaxial polydactyly, thumb and/or radius hypoplasia/agenesis, or triphalangeal thumb. Cardiac, pulmonary, renal, and central nervous system involvement has also been reported.
Disease Hierarchy
DISYKSRF: Genetic disease
DISHPNVX: Dysplasia
DISD0WVL: Multiple congenital anomalies/dysmorphic syndrome without intellectual disability
DIS0SIK5: Oculoauriculovertebral spectrum with radial defects
Disease Identifiers
MONDO ID
MONDO_0007712
MESH ID
D006053
UMLS CUI
C0220681
OMIM ID
141400
MedGen ID
67392
Orphanet ID
2549
SNOMED CT ID
726722009